5-Nitro-1-tetralone

5-Nitro-1-tetralone Suppliers list
Company Name: Beijing HwrkChemical Technology Co., Ltd  
Tel: 89508211 18501085097
Email: sales.bj@hwrkchemical.com
Company Name: BeiJing Hwrk Chemicals Limted  
Tel: 0757-86329057 18934348241
Email: sales4.gd@hwrkchemical.com
Company Name: Capot Chemical Co., Ltd  
Tel: +86 (0) 571 85 58 67 18
Email:
Company Name: Tetranov Biopharm  
Tel: 13526569071
Email: sales@leadmedpharm.com
Company Name: Shanghai Ennopharm Co., Ltd.  
Tel: +86 (21) 6435-5022
Email:

5-Nitro-1-tetralone manufacturers

  • 5-Nitro-1-tetralone
  • 5-Nitro-1-tetralone pictures
  • 2022-01-04
  • CAS:51114-73-9
  • Min. Order: 1g
  • Purity: 98%minHPLC
  • Supply Ability: 100kgs/month
5-Nitro-1-tetralone Basic information
Product Name:5-Nitro-1-tetralone
Synonyms: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)
CAS:51114-73-9
MF:C10H9NO3
MW:191.18
EINECS:
Product Categories:
Mol File:51114-73-9.mol
5-Nitro-1-tetralone Structure
5-Nitro-1-tetralone Chemical Properties
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
AppearanceWhite to light yellow Solid
Safety Information
MSDS Information
5-Nitro-1-tetralone Usage And Synthesis
Synthesis Reference(s)Journal of Medicinal Chemistry, 19, p. 472, 1976 DOI: 10.1021/jm00226a004
Synthesis
4-(2-NITRO-PHENYL)-BUTYRIC ACID

67857-97-0

5-Nitro-1-tetralone

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: US2003/176722, 2003, A1
5-Nitro-1-tetralone Preparation Products And Raw materials
Raw materialsBenzenebutanoyl chloride, 2-nitro--->4-(2-Nitro-phenyl)-butyric acid-->1-Tetralone
Preparation Products7-Nitro-1-tetralone-->5-Amino-1-naphthol
Tag:5-Nitro-1-tetralone(51114-73-9) Related Product Information
7-Nitro-1-tetralone,97%,7-NITRO-1-TETRALONE 5-Amino-3,4-dihydronaphthalen-1(2H)-one 8-Nitro-2-tetralone 7-Nitro-2-tetralone 8-Nitro-1-tetralone,8-Nitro-α-tetralone 6-Nitro-2-tetralone 6-NITRO-A-TETRALONE,6-Nitro-α-Tetralone,6-Nitro-1-tetralone 5-Nitro-2-tetralone Nitrocycline 5-Nitro-1-tetralone