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103-94-6

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103-94-6 Usage

General Description

2-((4-Nitrophenyl)amino)-2-oxoacetic acid is a chemical compound with the molecular formula C8H6N2O6. It consists of an oxoacetic acid group (-COCH2COOH) with a 4-nitroaniline moiety (4-nitrophenylamino) attached to one of its carbon atoms. It is of interest in organic chemistry and may have applications in various chemical reactions or as an intermediate in the synthesis of other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 103-94-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 103-94:
(5*1)+(4*0)+(3*3)+(2*9)+(1*4)=36
36 % 10 = 6
So 103-94-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O5/c11-7(8(12)13)9-5-1-3-6(4-2-5)10(14)15/h1-4H,(H,9,11)(H,12,13)

103-94-6 Well-known Company Product Price

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  • Alfa Aesar

  • (L00325)  4-Nitrophenyloxamic acid, 98%   

  • 103-94-6

  • 1g

  • 220.0CNY

  • Detail
  • Alfa Aesar

  • (L00325)  4-Nitrophenyloxamic acid, 98%   

  • 103-94-6

  • 5g

  • 724.0CNY

  • Detail

103-94-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-NITROPHENYLOXAMIC ACID

1.2 Other means of identification

Product number -
Other names 2-(4-nitroanilino)-2-oxoacetic acid

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:103-94-6 SDS

103-94-6Relevant articles and documents

Cerium (IV) mediated oxidative dimerization of 3-oxoacid anilides and their cyclizations

Zaleska,Lis

, p. 189 - 197 (2007/10/03)

Investigation of the behavior of several anilides of 3-oxoacids in oxidation reaction with ceric ammonium nitrate has shown that selective intermolecular C-C bond formation, which led to their dimers, is typical of these compounds. These dimeric species were cyclized in two routes, A and B, leading to 3-[2′-(1′-aniline-3′-oxo)-indene]-quinoline-2-on derivatives with HCl(g) (Route A), and with application of H2SO4 as a cyclization agent, gave furane-3,4-dicarboxylic acid derivatives (Route B).

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