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Ethyl 4-broMo-1-benzothiophene-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93103-82-3

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93103-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93103-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,0 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93103-82:
(7*9)+(6*3)+(5*1)+(4*0)+(3*3)+(2*8)+(1*2)=113
113 % 10 = 3
So 93103-82-3 is a valid CAS Registry Number.

93103-82-3Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS, PROCESS FOR PREPARATION OF THE SAME AND USE THEREOF

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, (2017/07/15)

The present invention provides a heterocyclic compound represented by the formula (I), its stereoisomers, or a pharmaceutically acceptable salt thereof, pharmaceutical compositions thereof, and their use in preparing a medicament for the prevention and/or treatment of central nervous system disease.

MODULATORS FOR NICOTINIC ACETYLCHOLINE RECEPTOR α2 AND α4 SUBUNITS

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Page/Page column 37; 38, (2016/12/22)

Positive allosteric modulators (PAMs) of nicotinic acetylcholine receptors (nAChR) are important therapeutic candidates as well as valuable research tools. We identified a novel type II PAM, (R)-7-bromo-N-(piperidin-3-yl)benzo[b]thiophene-2-carboxamide (B

Drug design, in vitro pharmacology, and structure-activity relationships of 3-acylamino-2-aminopropionic acid derivatives, a novel class of partial agonists at the glycine site on the N-methyl-D-aspartate (NMDA) receptor complex

Urwyler, Stephan,Floersheim, Philipp,Roy, Bernard L.,Koller, Manuel

supporting information; experimental part, p. 5093 - 5107 (2010/03/02)

Retaining agonistic activity at the glycine coagonist site of the NMDA receptor in molecules derived from glycine or D-serine has proven to be difficult because in the vicinity of the α-amino acid group little substitution is tolerated. We have solved thi

Condensed Heterocyclics: Part XVI - Synthesis of N-Substituted 4-Bromo-2-guanidinomethylbenzothiophenes

Sharma, K. S.,Lata, Suman

, p. 38 - 41 (2007/10/02)

4-Bromo-2-chloromethylbenzothiophene (V) and 4-bromobenzothiophene-2-carboxamides (VII, XI) have been converted into 2-aminomethyl- and 2-(N-methyl)aminomethyl-benzothiophenes (VIII, XII).The amine (VIII) has been transformed into N-substituted 2-guanidinomethylbenzothiophenes (IX) by reaction with appropriate N-substituted S-methylisothioureas.

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