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1027082-25-2

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1027082-25-2 Usage

General Description

4-Amino-7H-pyrrolo[2,3-d]pyrimidine-2-sulfinic acid is a chemical compound with the molecular formula C6H6N4O3S. It is a sulfinic acid derivative of pyrrolopyrimidine and contains an amino group, making it an important building block in organic synthesis. 4-Amino-7H-pyrrolo[2,3-d]pyrimidine-2-sulfinic acid has potential pharmaceutical applications and has been studied for its potential medicinal properties. It is used in the synthesis of various pharmaceutical compounds and is an important intermediate in the production of drugs. This chemical compound plays a crucial role in the development of new drugs and has potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1027082-25-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,0,8 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1027082-25:
(9*1)+(8*0)+(7*2)+(6*7)+(5*0)+(4*8)+(3*2)+(2*2)+(1*5)=112
112 % 10 = 2
So 1027082-25-2 is a valid CAS Registry Number.

1027082-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Amino-7H-pyrrolo[2,3-d]pyrimidine-2-sulfinic acid

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:1027082-25-2 SDS

1027082-25-2Relevant articles and documents

Practical synthesis of a potent hepatitis C virus RNA replication inhibitor

Bio, Matthew M.,Xu, Feng,Waters, Marjorie,Williams, J. Michael,Savary, Kimberly A.,Cowden, Cameron J.,Yang, Chunhua,Buck, Elizabeth,Song, Zhiguo J.,Tschaen, David M.,Volante,Reamer, Robert A.,Grabowski, Edward J. J.

, p. 6257 - 6266 (2007/10/03)

A practical, efficient synthesis of 1, a hepatitis C virus RNA replication inhibitor, is described. Starting with the inexpensive diacetone glucose, the 12-step synthesis features a novel stereoselective rearrangement to prepare the key crystalline furanose diol intermediate. This is followed by a highly selective glycosidation to couple the C-2 branched furanose epoxide with deazapurine.

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