ChemicalBook > CAS DataBase List > 5-Chloro-1-indanone

5-Chloro-1-indanone

Product Name
5-Chloro-1-indanone
CAS No.
42348-86-7
Chemical Name
5-Chloro-1-indanone
Synonyms
5-Chloro-2,3-dihydro-1H-inden-1-one;Chloro-1-indan;5-Chloro Indanone;5- chlorineindone;5-CHLORO-1-INDANONE;5-CHLOROINDAN-1-ONE;1-Indanone, 5-chloro-;5-Chloro-1-indanone,98%;5-Chloro-1-indanone,99%;5-Chloro-1-indanone >
CBNumber
CB2148511
Molecular Formula
C9H7ClO
Formula Weight
166.6
MOL File
42348-86-7.mol
More
Less

5-Chloro-1-indanone Property

Melting point:
94-98 °C (lit.)
Boiling point:
124-125 °C (3 mmHg)
Density 
1.1466 (rough estimate)
refractive index 
1.6000 (estimate)
Flash point:
124-125°C/3mm
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly)
form 
Solid
color 
Light Beige to Beige
Water Solubility 
insoluble
BRN 
1448000
InChIKey
MEDSHTHCZIOVPU-UHFFFAOYSA-N
CAS DataBase Reference
42348-86-7(CAS DataBase Reference)
NIST Chemistry Reference
5-Chloro-1-indanone(42348-86-7)
EPA Substance Registry System
1H-Inden-1-one, 5-chloro-2,3-dihydro- (42348-86-7)
More
Less

Safety

Hazard Codes 
Xn,Xi
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36
WGK Germany 
3
Hazard Note 
Irritant
TSCA 
Yes
HS Code 
29339900
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

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

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

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
433071
Product name
5-Chloro-1-indanone
Purity
99%
Packaging
5g
Price
$62.3
Updated
2024/03/01
TCI Chemical
Product number
C1644
Product name
5-Chloro-1-indanone
Purity
>97.0%(GC)
Packaging
1g
Price
$65
Updated
2024/03/01
TCI Chemical
Product number
C1644
Product name
5-Chloro-1-indanone
Purity
>97.0%(GC)
Packaging
5g
Price
$212
Updated
2024/03/01
Alfa Aesar
Product number
A18308
Product name
5-Chloro-1-indanone, 99%
Packaging
1g
Price
$46.65
Updated
2024/03/01
Alfa Aesar
Product number
A18308
Product name
5-Chloro-1-indanone, 99%
Packaging
5g
Price
$180.65
Updated
2024/03/01
More
Less

5-Chloro-1-indanone Chemical Properties,Usage,Production

Chemical Properties

White Crystal

Uses

5-Chloro-1-indanone is the important intermediate of du pont company's new varieties of pesticides indoxacarb (popular name: indoxacarb), is also a kind of important medicine intermediate simultaneously.
5-Chloro-1-indanone is a 5-halo-1-indanone. It participates in the Irie′s synthesis of substituted pyridines. 5-Chloro-1-indanone has a stable triclinic crystal structure and has intermolecular forces of C-H...O, C-H...Π, CO...Cl and Π...Π types.
5-Chloro-1-indanone may be used as starting reagent for the preparation of 5-chloro-2-methoxycarbonyl-1-indanone. It may be used for the preparation of important biomedical compounds such as anticonvulsants, anticholinergics and diarylsulfonylureas, having potential activity against solid tumors.

Uses

5-Chloro-1-indanone may be used as starting reagent for the preparation of 5-chloro-2-methoxycarbonyl-1-indanone. It may also be used for the preparation of important biomedical compounds such as anticonvulsants, anticholinergics and diarylsulfonylureas, having potential activity against solid tumors. It participates in the Irie?s synthesis of substituted pyridines.

Preparation

3-chlorobenzaldehyde as raw material first reacts with propionic acid to prepare 3-chloro-phenylpropionic acid, which is then subjected to Friedel-Crafts acylation reaction to prepare 5-chloro-1-indanone. Organic solvents of formic acid diethylamine participate in the first step, and the reaction temperature is 20-150℃. An organic solvent of methylene chloride and a catalyst of zinc chloride participate in the second step, and the reaction temperature is -10 to 80 ℃.
Synthetic method of 5-chloro-1-indanone

General Description

5-Chloro-1-indanone is a 5-halo-1-indanone. It participates in the Irie′s synthesis of substituted pyridines. 5-Chloro-1-indanone has a stable triclinic crystal structure and has intermolecular forces of C-H...O, C-H...Π, CO...Cl and Π...Π types.

5-Chloro-1-indanone Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

5-Chloro-1-indanone Suppliers

HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
AbaChemScene
Tel
732-484-9848
Fax
888-484-5008
Email
sales@chemscene.com
Country
United States
ProdList
3982
Advantage
60
Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63687
Advantage
58
AB PharmaTech,LLC
Tel
323-480-4688
Fax
323-480-4688
Email
sales@acrospharmatech.com
Country
United States
ProdList
989
Advantage
55
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Aceschem Inc.
Tel
+1-817863-6948 +1-(817)863-6948
Email
sales@aceschem.com
Country
United States
ProdList
19632
Advantage
58
Synthonix Inc
Tel
--
Fax
--
Email
info@synthonix.com
Country
United States
ProdList
6872
Advantage
58
Abblis Chemicals LLC
Tel
--
Fax
--
Email
info@abblis.com
Country
United States
ProdList
1272
Advantage
0
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
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
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
Reddy Chemtech Inc.
Tel
--
Fax
--
Email
sales@reddychemtech.com
Country
United States
ProdList
224
Advantage
0
Rintech, Inc.
Tel
--
Fax
--
Email
info@rintechinc.com
Country
United States
ProdList
3416
Advantage
60
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6962
Advantage
56
AlliChem, LLC
Tel
--
Fax
--
Email
sales@allichemllc.com
Country
United States
ProdList
6516
Advantage
60
Combi-Blocks Inc.
Tel
--
Fax
--
Email
sales@combi-blocks.com
Country
United States
ProdList
6618
Advantage
69
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
United States
ProdList
6814
Advantage
81
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
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
Chemiplus Corporation
Tel
--
Fax
--
Email
okazaki@chemiplus.com
Country
United States
ProdList
3198
Advantage
38
Syntech Labs
Tel
--
Fax
--
Email
info@syntechlabs.com
Country
United States
ProdList
730
Advantage
43
Ivy Fine Chemicals
Tel
--
Fax
--
Email
sales@ivychem.com
Country
United States
ProdList
6493
Advantage
58
Chontech, Inc.
Tel
--
Fax
--
Email
chontech@yahoo.com
Country
United States
ProdList
1101
Advantage
30
BOSCHE SCIENTIFIC, LLC
Tel
--
Fax
--
Email
Sales@BoscheSci.com
Country
United States
ProdList
6477
Advantage
55
Davos Chemical Corporation
Tel
--
Fax
--
Email
info@davos.com
Country
United States
ProdList
1640
Advantage
65
ChemPacific Corporation
Tel
--
Fax
--
Email
sales@chempacific.com
Country
United States
ProdList
6891
Advantage
51
Albemarle Corporation
Tel
--
Fax
--
Country
United States
ProdList
253
Advantage
81
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
Beta Pharma, Inc.
Tel
--
Fax
--
Email
sales@betapharma.com
Country
United States
ProdList
6226
Advantage
60
ASDI Incorporated
Tel
--
Fax
--
Email
customerservice@asdi.net
Country
United States
ProdList
6922
Advantage
67
More
Less

View Lastest Price from 5-Chloro-1-indanone manufacturers

Hebei Mujin Biotechnology Co.,Ltd
Product
5-Chloro-1-indanone 42348-86-7
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-08-30
Hebei Zhuanglai Chemical Trading Co Ltd
Product
5-Chloro-1-indanone 42348-86-7
Price
US $10.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20 ton
Release date
2024-12-13
Hebei Weibang Biotechnology Co., Ltd
Product
5-Chloro-1-indanone 42348-86-7
Price
US $8.90/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2024-11-28

42348-86-7, 5-Chloro-1-indanoneRelated Search:


  • 5-chloro-2,3-dihydroinden-1-one
  • 5-Chloro-1-indanone,98%
  • 1-Indanone, 5-chloro-5- chlorineindon
  • 5 - chlorine indene ketone
  • Chloro-1-indan
  • 5-CHLORO-1-INDANONE
  • 5-CHLOROINDAN-1-INDANONE
  • 5-CHLOROINDAN-1-ONE
  • 1H-Inden-1-one, 5-chloro-2,3-dihydro-
  • 1-Indanone, 5-chloro-
  • 5-Chloro-2,3-dihydro-1H-inden-1-one
  • 5-Chloro-1-indanone,99%
  • 5-Chloro Indanone
  • 5- chlorineindone
  • 5-Chloro-1-indanone &gt
  • 1-Indanone,5-chloro- (7CI)
  • 2,3- dihydro -5- chloroindolone
  • Indoxacarb intermediate
  • 42348-86-7
  • C9H7OCl
  • Organic Building Blocks
  • Ketones
  • Building Blocks
  • Carbonyl Compounds
  • C9
  • Building Blocks
  • C9
  • Carbonyl Compounds
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks
  • Benzocycles
  • Indane/Indanone and Derivatives
  • Ketones
  • Indanone & Indene
  • 42348-86-7