ChemicalBook > CAS DataBase List > 2-Indanone

2-Indanone

Product Name
2-Indanone
CAS No.
615-13-4
Chemical Name
2-Indanone
Synonyms
1,3-Dihydro-2H-inden-2-one;Indan-2-one;1H-inden-2(3H)-one;2-lndanone;2-Indene;2-INDANONE;2-OXOINDANE;2-indanones;2-Hydrindone;INDANONE(2-)
CBNumber
CB6711313
Molecular Formula
C9H8O
Formula Weight
132.16
MOL File
615-13-4.mol
More
Less

2-Indanone Property

Melting point:
51-54 °C (lit.)
Boiling point:
218°C
Density 
1.0712
refractive index 
1.5380 (estimate)
Flash point:
212 °F
storage temp. 
2-8°C
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly)
form 
Crystals or Powder
color 
Light yellow to yellow-brown
Specific Gravity
1.07 (liquid)
Odor
moderately tenacious odor
Odor Threshold
0.00036ppm
Water Solubility 
insoluble
Sensitive 
Hygroscopic
BRN 
636550
InChIKey
UMJJFEIKYGFCAT-UHFFFAOYSA-N
LogP
1.230 (est)
CAS DataBase Reference
615-13-4(CAS DataBase Reference)
NIST Chemistry Reference
2H-inden-2-one, 1,3-dihydro-(615-13-4)
EPA Substance Registry System
2-Indanone (615-13-4)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
22-24/25-36-26
WGK Germany 
3
RTECS 
NK7535500
F 
3
Hazard Note 
Irritant
TSCA 
Yes
HS Code 
29145090
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
146692
Product name
2-Indanone
Purity
98%
Packaging
10g
Price
$214
Updated
2024/03/01
TCI Chemical
Product number
I0649
Product name
2-Indanone
Purity
>98.0%(GC)
Packaging
5g
Price
$49
Updated
2024/03/01
TCI Chemical
Product number
I0649
Product name
2-Indanone
Purity
>98.0%(GC)
Packaging
25g
Price
$90
Updated
2024/03/01
Alfa Aesar
Product number
A12574
Product name
2-Indanone, 98%
Packaging
5g
Price
$50.65
Updated
2024/03/01
Alfa Aesar
Product number
A12574
Product name
2-Indanone, 98%
Packaging
25g
Price
$192
Updated
2023/06/20
More
Less

2-Indanone Chemical Properties,Usage,Production

Chemical Properties

Wet crystalline aggregates or needle-like crystals (formed by ethanol or ether) evaporate when in contact with water vapor. These crystals have a melting point range of 58-61 ℃ and a flash point of 100 ℃. Indene compounds are commonly found in numerous natural products, exhibiting diverse physiological activities and serving as crucial intermediates in organic synthesis processes.

Uses

2-Indanone undergoes TiCl4-Mg mediated coupling with CHBr3 to yield dibromomethyl carbinol. It reacts with 5,5-dimethyl-3-pyrazolidinone to yield 5,5-dimethyl-2-(1H-indenyl-2)-3-pyrazolidinone. On photolysis by 266-nm one-photon excitation yields o-xylylene. It was used as starting reagent in the synthesis of indene-fused porphyrins.

Preparation

2-Indanone is prepared by using acetic acid as solvent, acetic anhydride as catalyst and through hydrogen peroxide oxidation into 1, 2-indenediol, which reacted with dilute sulfuric acid solution in order to obtain crude 2-indanone. Finally, vacuum sublimation to obtain 2-indanone with high-purity, the total yield is 89%.

Definition

ChEBI: 2-Indanone is an indanone with an oxo substituent at position 2. It is a metabolite of indane. It has a role as a xenobiotic metabolite. 2-Indanone is an intermediate for the preparation of aprindine hydrochloride and ceforanide. It is an important intermediate in organic synthesis.

Application

2-Indanone is mentioned mainly for the completion and illustration of the series in which dpila- and be{u-Hydrindone have been emphasized as having potential interest in the perfume industry. It is the author's impression that the two materials are not used in perfumes or flavors.

Synthesis Reference(s)

Chemistry Letters, 11, p. 325, 1982
Organic Syntheses, Coll. Vol. 5, p. 647, 1973
Tetrahedron Letters, 15, p. 3789, 1974 DOI: 10.1016/S0040-4039(01)92010-6

General Description

2-Indanone undergoes TiCl4-Mg mediated coupling with CHBr3 to yield dibromomethyl carbinol. It reacts with 5,5-dimethyl-3-pyrazolidinone to yield 5,5-dimethyl-2-(1H-indenyl-2)-3-pyrazolidinone. 2-Indanone on photolysis by 266-nm one-photon excitation yields o-xylylene.

2-Indanone Preparation Products And Raw materials

Raw materials

Preparation Products

3-Isochromanone DELAPRIL
More
Less

2-Indanone Suppliers

Americas 1 Belgium 6 China 332 Europe 4 France 2 Germany 7 India 29 Japan 8 Slovakia 1 South Korea 1 Switzerland 4 The Netherlands 1 United Kingdom 20 United States 60 Global 476
Ark Pharm, Inc.
Tel
847-367-3680
Fax
847-367-3681
Email
sales@arkpharminc.com
Country
United States
ProdList
1670
Advantage
56
Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Fax
001-617-206-9595
Email
sales@chemreagents.com
Country
United States
ProdList
10186
Advantage
62
BOC Sciences
Tel
1-631-485-4226; 16314854226
Email
info@bocsci.com
Country
United States
ProdList
14055
Advantage
65
HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Accela ChemBio Inc.
Tel
+1(858) 699-3322
Fax
+1(858) 876-1948
Email
marketing@accelachem.com
Country
United States
ProdList
6024
Advantage
65
AbaChemScene
Tel
732-484-9848
Fax
888-484-5008
Email
sales@chemscene.com
Country
United States
ProdList
3982
Advantage
60
Accela ChemBio Inc.
Tel
+1-858-6993322
Fax
(+1)-858-876-1948
Email
info@accelachem.com
Country
United States
ProdList
17777
Advantage
58
Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63687
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Aston Chemical
Tel
13000000000
Email
sales@astonchem.com
Country
United States
ProdList
1634
Advantage
58
Alfa Chemistry
Tel
Email
info@alfa-chemistry.com
Country
United States
ProdList
2344
Advantage
58
Combi-Blocks, Inc.
Tel
--
Fax
--
Email
les@combi-blocks.com
Country
United States
ProdList
2555
Advantage
58
2A Biotech USA
Tel
--
Fax
--
Email
info@2abiotech.com
Country
United States
ProdList
1785
Advantage
58
MilliporeSigma (Sigma-Aldrich Corp.)
Tel
--
Fax
--
Email
@sial.com
Country
United States
ProdList
5414
Advantage
58
Crescent Chemical Company
Tel
--
Fax
--
Email
fran@creschem.com
Country
United States
ProdList
1441
Advantage
58
Fluorochem Ltd.
Tel
--
Fax
--
Email
enquiries@fluorochem.co.uk
Country
United States
ProdList
4583
Advantage
58
Alichem Inc.
Tel
--
Fax
--
Email
sales@alichem.com
Country
United States
ProdList
6167
Advantage
58
MP Biomedicals, LLC. (Division of Valiant FC Co., Ltd.)
Tel
--
Fax
--
Email
serv@mpbio.com
Country
United States
ProdList
1854
Advantage
58
eNovation Chemicals LLC
Tel
--
Fax
--
Email
ales@eNovationChem.com
Country
United States
ProdList
1673
Advantage
58
Chem-Impex International, Inc. (CII)
Tel
--
Fax
--
Email
Customer@chemimpex.com
Country
United States
ProdList
893
Advantage
58
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
TCI America, Inc. (part of Tokyo Chemical Industry)
Tel
--
Fax
--
Email
Angelina.Crew@tcichemicals.com
Country
United States
ProdList
2053
Advantage
58
Spectrum Chemicals & Laboratory Products
Tel
--
Fax
--
Email
sales@spectrumchemical.com
Country
United States
ProdList
6699
Advantage
77
Accela ChemBio Inc.
Tel
--
Fax
--
Email
info@accelachem.com
Country
United States
ProdList
1054
Advantage
50
VWR International, LLC.
Tel
--
Fax
--
Email
@sargentwelch.com
Country
United States
ProdList
6262
Advantage
58
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
SynQuest Laboratories, Inc.
Tel
--
Fax
--
Email
info@synquestlabs.com
Country
United States
ProdList
6871
Advantage
62
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Frontier Scientific, Inc.
Tel
--
Fax
--
Email
sales@frontiersci.com
Country
United States
ProdList
6222
Advantage
86
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Alfa Chemistry
Tel
--
Fax
--
Email
info@Alfa-Chemistry.com
Country
United States
ProdList
6814
Advantage
0
Anisyn, Inc.
Tel
--
Fax
--
Email
sales@anisyn.com
Country
United States
ProdList
863
Advantage
0
Fisher Scientific
Tel
--
Fax
--
Email
sales@fishersci.com
Country
United States
ProdList
2337
Advantage
86
Sisco Research Laboratories Pvt. Ltd.
Tel
--
Fax
--
Email
srlmarketing@dishnetdsl.net
Country
United States
ProdList
1905
Advantage
64
HBCChem Inc.
Tel
--
Fax
--
Email
sales@hbcchem-inc.com
Country
United States
ProdList
4569
Advantage
30
HDH Pharma, Inc.
Tel
--
Fax
--
Email
catalog@hdhpharma.com
Country
United States
ProdList
6248
Advantage
62
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6962
Advantage
56
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
AlliChem, LLC
Tel
--
Fax
--
Email
sales@allichemllc.com
Country
United States
ProdList
6516
Advantage
60
Parish Chemical Company
Tel
--
Fax
--
Country
United States
ProdList
1248
Advantage
47
Advanced Synthesis Technologies
Tel
--
Fax
--
Email
sales@advancedsynthesis.com
Country
United States
ProdList
4775
Advantage
61
Chem-Impex International, Inc.
Tel
--
Fax
--
Country
United States
ProdList
6730
Advantage
64
ChemSampCo, Inc.
Tel
--
Fax
--
Email
sales@chemsampco.com
Country
United States
ProdList
3585
Advantage
60
George Uhe Co., Inc.
Tel
--
Fax
--
Email
global@uhe.com
Country
United States
ProdList
520
Advantage
65
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
United States
ProdList
6814
Advantage
81
2A PharmaChem USA
Tel
--
Fax
--
Email
sales@2apharmachem.com
Country
United States
ProdList
6137
Advantage
39
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
Bio-Vin Research Laboratories
Tel
--
Fax
--
Email
sales@biovinresearch.com
Country
United States
ProdList
6210
Advantage
64
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
More
Less

View Lastest Price from 2-Indanone manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
2-Indanone 615-13-4
Price
US $0.00/KG
Min. Order
1KG
Purity
98%min
Supply Ability
30tons/month
Release date
2023-04-07
Hebei Yanxi Chemical Co., Ltd.
Product
2-Indanone 615-13-4
Price
US $1.00/kg
Min. Order
1kg
Purity
99.00%
Supply Ability
20tons
Release date
2023-09-06
Hebei Chuanghai Biotechnology Co,.LTD
Product
2-Indanone 615-13-4
Price
US $5.00-2.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10000kg
Release date
2024-08-23

615-13-4, 2-IndanoneRelated Search:

Indan 1,2-Indanedione 4-Chloro-2-indanone 5-Nitro-2-indanone INDANONE,INDANONE(1-),1-INDANONE,2,3-Dihydro-1-indanone,alpha-Indanone 2H-INDEN-2-ONE, 1,3-DIHYDRO-5-METHOXY- 4-Methoxy-2-indanone 4-Bromo-2-indanone 5-Bromo-2-indanone 5-Fluoro-2-indanone 5-Chloro-2-indanone 5-Bromo-1-indanone 6-Iodo-1-Indanone 7-METHOXY-1-INDANONE 97 6-Cyano-1-indanone 4-Chloro-1-Indanone 4-Nitro-1-Indanone 4-METHOXY-1-INDANONE

  • 1,3-dihydro-2h-inden-2-on
  • 1,3-Dihydro-2H-inden-2-one
  • 2H-Inden-2-one,1,3-dihydro-
  • 2-Hydrindone
  • 2-Oxohydrindene
  • 2-INDANONE
  • INDANONE(2-)
  • Indan-2-one
  • BETA-HYDRINDONE
  • 1H-inden-2(3H)-one
  • 2-INDANONE pure
  • 2-OXOINDANE
  • 2-lndanone
  • 2-Indanone,98%
  • Indan-2-one 98%
  • 1,3-dihydroinden-2-one
  • 2-Indanone,97%
  • 2-Indanone, 97% 10GR
  • beta-Hydrindone 2-Oxoindane
  • 2-indanones
  • 2-Indanone Vetec(TM) reagent grade, 98%
  • 2 - indene ketone
  • 2-Indanone&gt
  • 2-Indanone (7CI, 8CI)
  • 2-Indene
  • 615-13-4
  • C9H8O
  • Organic Building Blocks
  • Ketones
  • Building Blocks
  • C9
  • Carbonyl Compounds
  • Indane/Indanone and Derivatives
  • Indanone & Indene
  • Carbonyl Compounds
  • bc0001
  • 615-13-4