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2-AMINO-N-BENZYL-5,6,7,8-TETRAHYDRO-4H-CYCLOHEPTA[B]THIOPHENE-3-CARBOXAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

588692-39-1

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  • 2-Amino-N-benzyl-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carboxamide

    Cas No: 588692-39-1

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588692-39-1 Usage

Properties

1. Chemical name: 2-Amino-N-benzyl-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carboxamide
2. Class: Carboxamides
3. Structure: Heterocyclic compound with a cyclic structure containing thiophene and cycloheptane rings
4. Functional groups: Amine and benzyl group
5. Potential applications: Pharmaceutical and medicinal chemistry, development of new materials and compounds with bioactive properties

Specific content

1. Chemical name: 2-Amino-N-benzyl-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carboxamide
2. Class: Carboxamides
3. Structure: Heterocyclic compound with a cyclic structure containing thiophene and cycloheptane rings
4. Functional groups: Amine and benzyl group
5. Potential applications: Pharmaceutical and medicinal chemistry, development of new materials and compounds with bioactive properties

Check Digit Verification of cas no

The CAS Registry Mumber 588692-39-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,8,6,9 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 588692-39:
(8*5)+(7*8)+(6*8)+(5*6)+(4*9)+(3*2)+(2*3)+(1*9)=231
231 % 10 = 1
So 588692-39-1 is a valid CAS Registry Number.

588692-39-1Downstream Products

588692-39-1Relevant articles and documents

2-Aminothiophene-3-carboxylates and carboxamides as adenosine A1 receptor allosteric enhancers

Nikolakopoulos, George,Figler, Heidi,Linden, Joel,Scammells, Peter J.

, p. 2358 - 2365 (2007/10/03)

Three series of 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene and 2-amino-5,6,7,8-tetrahydrocyclohepta[b]thiophenes with 3-carboxylates and carboxamides have been prepared using the Gewald synthesis and evaluated as A1AR allosteric enhancers. The

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