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369-36-8

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369-36-8 Usage

Chemical Properties

ochre-yellow to light brown crystalline powder

Uses

It is employed as pharmaceutical intermediate.

Synthesis Reference(s)

Tetrahedron Letters, 31, p. 6141, 1990 DOI: 10.1016/S0040-4039(00)97008-4

Check Digit Verification of cas no

The CAS Registry Mumber 369-36-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 369-36:
(5*3)+(4*6)+(3*9)+(2*3)+(1*6)=78
78 % 10 = 8
So 369-36-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H5FN2O2/c7-5-2-1-4(9(10)11)3-6(5)8/h1-3H,8H2

369-36-8 Well-known Company Product Price

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  • Alfa Aesar

  • (A17545)  2-Fluoro-5-nitroaniline, 98+%   

  • 369-36-8

  • 25g

  • 552.0CNY

  • Detail
  • Alfa Aesar

  • (A17545)  2-Fluoro-5-nitroaniline, 98+%   

  • 369-36-8

  • 100g

  • 1803.0CNY

  • Detail

369-36-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluoro-5-nitroaniline

1.2 Other means of identification

Product number -
Other names 3-Amino-4-fluoronitrobenzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:369-36-8 SDS

369-36-8Relevant articles and documents

Lawrence,Ferguson

, p. 1220,1223 (1960)

Selective partial hydrogenation of dinitrobenzenes to nitroanilines catalyzed by Ru/C

Hou, Jie,Ma, Yonghuan,Li, Yuhan,Guo, Fang,Lu, Lianhai

scheme or table, p. 974 - 975 (2009/04/06)

Ru/C was found to be a highly effective catalyst for the selective partial hydrogenation of a range of dinitrobenzenes to their corresponding nitroanilines with excellent selectivity under mild conditions. Furthermore, the effect from other substitute groups of dinitrobenzenes on partial hydrogenation was also explored in this study. Copyright

Catalytic reduction of dinitrobenzenes using a noble metal catalyst and iron or iron salts

-

, (2008/06/13)

There is provided an improved process for the reduction of optionally substituted dinitrobenzenes to the corresponding nitroanilines with high yields which comprises contacting the dinitrobenzene with hydrogen in an acidic medium in the presence of a catalytic amount of a combination of a noble metal hydrogenation catalyst, and iron or an iron salt. Isomer specific reductions may be achieved with those compounds containing suitable directing substituents. The 2-halo-5-nitroanilines which may be produced in this process may be converted via a multi-step synthesis to useful 1-aryl-4-substituted 1,4-dihydro-5H-tetrazol-5-one herbicides.

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