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31055-19-3

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  • Allopurinol Related Compound E (25 mg) (ethyl 5-(formylamino)-1H-pyrazole-4-carboxylate)

    Cas No: 31055-19-3

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31055-19-3 Usage

Description

Ethyl 5-(formylamino)-1H-pyrazole-4-carboxylate, also known as 3-(Formylamino)-1H-pyrazole-4-carboxylic Acid Ethyl Ester, is an impurity of Allopurinol, a pyrazole derivative with potential applications in inducing neoplasm immunogenicity.

Uses

Used in Pharmaceutical Industry:
Ethyl 5-(formylamino)-1H-pyrazole-4-carboxylate is used as an impurity in Allopurinol, a medication primarily used for the treatment of gout and hyperuricemia. Its presence in Allopurinol may contribute to the drug's therapeutic effects or require monitoring and control to ensure safety and efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 31055-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,5 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 31055-19:
(7*3)+(6*1)+(5*0)+(4*5)+(3*5)+(2*1)+(1*9)=73
73 % 10 = 3
So 31055-19-3 is a valid CAS Registry Number.

31055-19-3 Well-known Company Product Price

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  • Sigma-Aldrich

  • (A0350050)  Allopurinol impurity E  European Pharmacopoeia (EP) Reference Standard

  • 31055-19-3

  • A0350050

  • 1,880.19CNY

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  • USP

  • (1013068)  Allopurinol Related Compound E  United States Pharmacopeia (USP) Reference Standard

  • 31055-19-3

  • 1013068-25MG

  • 13,501.80CNY

  • Detail

31055-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 5-formamido-1H-pyrazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names Allopurinol Impurity E

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:31055-19-3 SDS

31055-19-3Downstream Products

31055-19-3Relevant articles and documents

Synthesis of 5-amino-4, 5-dihydropyrazolo [3,4-d] pyrimidin-4-ones and related isomeric systems. Part I. Synthesis and characterization of potential intermediates

Maquestiau,Vanden Eynde

, p. 4185 - 4193 (2007/10/02)

Reactions between aminopyrazole-4-carboxylic acids derivatives and orthoesters or amide acetals lead, in most cases, to the introduction of a heteroalkylidene moiety on the amino group of ethyl aminopyrazole-4-carboxylates and on the β-hydrazide nitrogen atom of aminopyrazole-4-carboxhydrazides. Several factors governing the course of these reactions are discussed.

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