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Sodium 2-(2-aminophenyl)-2-oxoacetate, also known as 2-(2-aminophenyl)glyoxylate sodium salt, is a chemical compound with the molecular formula C8H5NNaO4. It is a derivative of oxoacetic acid and is commonly used as an intermediate in the synthesis of pharmaceuticals and organic compounds. sodiuM 2-(2-aMinophenyl)-2-oxoacetate is a white to off-white crystalline powder that is soluble in water. It is primarily used in research and development for its potential application in the pharmaceutical industry, particularly in the development of drugs targeting the central nervous system and related disorders.

17617-34-4

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17617-34-4 Usage

Uses

Used in Pharmaceutical Industry:
Sodium 2-(2-aminophenyl)-2-oxoacetate is used as an intermediate in the synthesis of pharmaceuticals for its potential application in the development of drugs targeting the central nervous system and related disorders.
Used in Organic Synthesis:
Sodium 2-(2-aminophenyl)-2-oxoacetate is used as a reagent in organic synthesis, contributing to the creation of various chemical intermediates.
Used in Research and Development:
sodiuM 2-(2-aMinophenyl)-2-oxoacetate is utilized in research and development settings to explore its properties and potential applications in the pharmaceutical and chemical industries, furthering the understanding of its role in drug development and synthesis processes.

Check Digit Verification of cas no

The CAS Registry Mumber 17617-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,1 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17617-34:
(7*1)+(6*7)+(5*6)+(4*1)+(3*7)+(2*3)+(1*4)=114
114 % 10 = 4
So 17617-34-4 is a valid CAS Registry Number.

17617-34-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Sodium 2-(2-aminophenyl)-2-oxoacetate

1.2 Other means of identification

Product number -
Other names sodium,2-(2-aminophenyl)-2-oxoacetate

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:17617-34-4 SDS

17617-34-4Upstream product

17617-34-4Relevant academic research and scientific papers

A new route to the synthesis of ellipticine quinone from isatin

Ramkumar, Nagarajan,Nagarajan, Rajagopal

, p. 1104 - 1106 (2014)

1-(2-Oxo-2-(pyridin-4-yl)ethyl)indoline-2,3-dione can be prepared and converted by treatment with sodium hydroxide into 2-isonicotinoyl-1H-indole-3- carboxylic acid as a key intermediate which can be transformed into ellipticine quinone in a two step sequ

One-pot three-component synthesis of novel 2-(3-nitro-phenyl)-quinazoline-4-carboxylic acid derivatives

Gok, Dervis

, p. 3343 - 3353 (2019)

A simple and easy synthesis of 2-(3-nitro-phenyl)-quinazoline-4-carboxylic acid (3) has been successfully developed through a one-pot three-component condensation reaction of (2-amino-phenyl)-oxo-acetic acid sodium salt (1) obtained from the hydrolysis of

A new route to the synthesis of ellipticine quinone from isatin

Ramkumar, Nagarajan,Nagarajan, Rajagopal

supporting information, p. 1104 - 1106 (2015/02/19)

1-(2-Oxo-2-(pyridin-4-yl)ethyl)indoline-2,3-dione can be prepared and converted by treatment with sodium hydroxide into 2-isonicotinoyl-1H-indole-3-carboxylic acid as a key intermediate which can be transformed into ellipticine quinone in a two step seque

A Simple Synthesis of 2-Acyl Indoles from Isatins

Black, David St. C.,Wong, Laurence C. H.

, p. 200 (2007/10/02)

N-Phenacyl- and N-acetonyl-isatins can be prepared and converted by treatment with sodium hydroxide into 2-acyl indoles and/or 2-acyl indole-3-carboxylic acids.

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