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185430-52-8

3-amino-4-(methoxymethyl)-6-methylthieno[2,3-b]pyridine-2-carboxamide is a complex organic compound with the molecular formula C12H14N2O3S. It belongs to the class of heterocyclic compounds, specifically a thieno[2,3-b]pyridine derivative, which is characterized by the presence of a thiophene ring fused to a pyridine ring. 3-amino-4-(methoxymethyl)-6-methylthieno[2,3-b]pyridine-2-carboxamide features an amino group at the 3-position, a methoxymethyl group at the 4-position, and a methyl group at the 6-position. The carboxamide group is attached at the 2-position, indicating its role as a carboxamide derivative. Such compounds are often studied for their potential pharmaceutical applications, including their interactions with biological targets and their effects on various physiological processes. The specific properties and applications of 3-amino-4-(methoxymethyl)-6-methylthieno[2,3-b]pyridine-2-carboxamide would depend on its chemical structure and the context in which it is being used or studied.

185430-52-8

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  • 3-Amino-4-(methoxymethyl)-6-methylthieno[2,3-b]pyridine-2-carboxamide

    Cas No: 185430-52-8

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185430-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 185430-52-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,4,3 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 185430-52:
(8*1)+(7*8)+(6*5)+(5*4)+(4*3)+(3*0)+(2*5)+(1*2)=138
138 % 10 = 8
So 185430-52-8 is a valid CAS Registry Number.

185430-52-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-4-(methoxymethyl)-6-methylthieno[2,3-b]pyridine-2-carboxamide

1.2 Other means of identification

Product number -
Other names HMS1484O04

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

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More Details:185430-52-8 SDS

185430-52-8Downstream Products

185430-52-8Relevant articles and documents

Synthesis of substituted 2-alkyl(aryl)thio-3-cyanopyridines and 3-aminothieno[2,3-b]pyridines

Kaigorodova,Konyushkin,Mikhailichenko,Vasilin,Kul'nevich

, p. 1234 - 1238 (1996)

The alkylation of 6-methyl-4-methoxymethyl-3-cyano-2(1H)pyridinethione by halogen derivatives in the presence of KOH proceeds regioselectively with the formation of S-alkyl derivatives. By cathodic electrolysis of the thiols in the presence of 6-methyl-4-

Reaction of vicinal thieno[2,3-b]pyridine aminoamides with Lawesson's reagent

Red'Kin,Stroganova,Vasilin,Krapivin

, p. 1701 - 1709 (2013/07/04)

The reaction of vicinal thieno[2,3-b]pyridine aminoamides with Lawesson's reagent gave new condensed diazaphosphinine derivatives. The structure of the substituent at the amide nitrogen atom and the reagent ratio were found to affect the direction of this

Some transformations of tertiary N-furfurylamides of aromatic and heteroaromatic carboxylic acids under acidic conditions

Stroganova, Tatyana A.,Vasilin, Vladimir K.,Zelenskaya, Elena A.,Red'kin, Viktor M.,Krapivin, Gennady D.

experimental part, p. 3088 - 3098 (2009/04/06)

Acid-catalyzed transformations of tertiary N-furfurylamides of ortho-amino substituted aromatic and heteroaromatic carboxylic acids accompanied by elimination of the furfuryl moiety are investigated. Georg Thieme Verlag Stuttgart.

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