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5-Nitro-1-tetralone

Product Name
5-Nitro-1-tetralone
CAS No.
51114-73-9
Chemical Name
5-Nitro-1-tetralone
Synonyms
5-NITRO-A-TETRALONE;5-Nitro-α-tetralone;5-Nitro-1-tetralone;5-Nitro-3,4-dihydronaphthalen-1(2H);5-nitro-3,4-dihydronaphthalen-1(2H)-one;3,4-dihydro-5-nitronaphthalen-1(2H)-one;5-Nitro-3,4-dihydro-2H-naphthalen-1-one;1(2H)-Naphthalenone, 3,4-dihydro-5-nitro-;5-nitro-1,2,3,4-tetrahydronaphthalen-1-one
CBNumber
CB8948030
Molecular Formula
C10H9NO3
Formula Weight
191.18
MOL File
51114-73-9.mol
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5-Nitro-1-tetralone Property

Melting point:
103-104 °C
Boiling point:
349.9±31.0 °C(Predicted)
Density 
1.322±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
Appearance
White to light yellow Solid
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
N901308
Product name
5-Nitro-3,4-dihydronaphthalen-1(2H)-one
Packaging
10mg
Price
$45
Updated
2021/12/16
ChemScene
Product number
CS-0060664
Product name
5-Nitro-3,4-dihydro-2H-naphthalen-1-one
Packaging
1g
Price
$50
Updated
2021/12/16
ChemScene
Product number
CS-0060664
Product name
5-Nitro-3,4-dihydro-2H-naphthalen-1-one
Packaging
5g
Price
$150
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
35462
Product name
5-Nitro-3,4-dihydronaphthalen-1(2H)-one
Purity
95+%
Packaging
250mg
Price
$572
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0078884
Product name
3,4-DIHYDRO-5-NITRONAPHTHALEN-1(2H)-ONE
Purity
95.00%
Packaging
5G
Price
$1212.75
Updated
2021/12/16
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5-Nitro-1-tetralone Chemical Properties,Usage,Production

Synthesis Reference(s)

Journal of Medicinal Chemistry, 19, p. 472, 1976 DOI: 10.1021/jm00226a004

Synthesis

67857-97-0

51114-73-9

The general procedure for the synthesis of 5-nitro-α-tetralone from 4-(2-nitrophenyl)butyric acid was as follows: first, 1 g of 4-(2-nitrophenyl)butyric acid (NPBS, 4.78 mmol) and 18 g of trifluoromethanesulfonic acid (TFMS) were added to a 100 mL two-necked flask fitted with a reflux condenser and magnetic stirrer at 20 °C. Under stirring, the reaction mixture was placed in an oil bath preheated to 130 °C and stirred continuously at this temperature for 45 min. Upon completion of the reaction, the mixture was cooled and transferred to a microdistillation unit. Most of the excess TFMS was removed by distillation at 52 °C and 0.5 mbar.After distillation, the bottom residue contained 0.914 g of 5-nitro-3,4-dihydro-1(2H)-naphthalenone and 3.44 g of TFMS (as determined by the GC-ISTD/internal standard method) in 99.3% yield, with 100% conversion to NPBS and 99.3% selectivity.

References

[1] Patent: EP1369412, 2003, A1. Location in patent: Page 6
[2] Patent: EP1369412, 2003, A1. Location in patent: Page 6
[3] Patent: US2003/176722, 2003, A1

5-Nitro-1-tetralone Preparation Products And Raw materials

Raw materials

Preparation Products

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5-Nitro-1-tetralone Suppliers

Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63687
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58
Aladdin Scientific
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Email
tp@aladdinsci.com
Country
United States
ProdList
57505
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58
Synthonix Inc
Tel
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Email
info@synthonix.com
Country
United States
ProdList
6872
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58
WBV international Limited
Tel
--
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Email
kelvin@webringvalue.com
Country
United States
ProdList
51
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Combi-Blocks Inc.
Tel
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Email
sales@combi-blocks.com
Country
United States
ProdList
6618
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69
SynChem,Inc
Tel
--
Fax
--
Email
sales@synchem.com
Country
United States
ProdList
4697
Advantage
58
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View Lastest Price from 5-Nitro-1-tetralone manufacturers

Shanghai Rlavie Technology Co ltd
Product
5-Nitro-1-tetralone 51114-73-9
Price
US $0.00-0.00/KG
Min. Order
1g
Purity
98%minHPLC
Supply Ability
100kgs/month
Release date
2021-11-17

51114-73-9, 5-Nitro-1-tetraloneRelated Search:


  • 5-Nitro-1-tetralone
  • 5-Nitro-α-tetralone
  • 5-NITRO-A-TETRALONE
  • 3,4-dihydro-5-nitronaphthalen-1(2H)-one
  • 5-nitro-3,4-dihydronaphthalen-1(2H)-one
  • 5-nitro-1,2,3,4-tetrahydronaphthalen-1-one
  • 5-Nitro-3,4-dihydro-2H-naphthalen-1-one
  • 5-Nitro-3,4-dihydronaphthalen-1(2H)
  • 1(2H)-Naphthalenone, 3,4-dihydro-5-nitro-
  • 51114-73-9