216985-67-0 Usage
Uses
Used in Pharmaceutical Industry:
[(3-CHLORO-BENZO[B]THIOPHENE-2-CARBONYL)-AMINO]-ACETIC ACID is used as a building block for the synthesis of various pharmaceutical compounds due to its unique structural features and potential biological activities. Its chemical properties allow for the creation of new drugs with improved efficacy and selectivity.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, [(3-CHLORO-BENZO[B]THIOPHENE-2-CARBONYL)-AMINO]-ACETIC ACID serves as a valuable molecule for the development of novel therapeutic agents. Its structural characteristics can be exploited to design drugs targeting specific biological pathways or receptors, potentially leading to more effective treatments for various diseases.
Used in Drug Discovery and Design:
[(3-CHLORO-BENZO[B]THIOPHENE-2-CARBONYL)-AMINO]-ACETIC ACID is utilized as a key component in drug discovery and design processes. Its unique chemical properties and potential pharmacological activities make it an attractive candidate for the development of innovative drugs with improved therapeutic profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 216985-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,9,8 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 216985-67:
(8*2)+(7*1)+(6*6)+(5*9)+(4*8)+(3*5)+(2*6)+(1*7)=170
170 % 10 = 0
So 216985-67-0 is a valid CAS Registry Number.
216985-67-0Relevant articles and documents
Synthesis and antimicrobial activity of oxazolone, imidazolone and triazine derivatives containing benzothiophene
Naganagowda, Gadada,Thamyongkit, Patchanita,Petsom, Amorn
experimental part, p. 794 - 804 (2012/01/05)
3-Chloro-1-benzothiophene-2-carbonylchloride (1) was allowed to react with glycine to give 3-chloro-1-benzothiophen-2-yl-carbonylaminoacetic acid (2). Various aldehydes were treated with compound (2) in acetic anhydride to get 1,3-oxazol-5-ones (3a-d). Th
Synthesis and antimicrobial activity of oxazolone, imidazolone and triazine derivatives containing benzothiophene
Naganagowda, Gadada,Petsom, Amorn
experimental part, p. 3914 - 3922 (2012/03/26)
3-Chloro-1-benzothiophene-2-carbonyl chloride 1 was reacted with glycine in acetone to give 3-chloro-1- benzothiophen-2-yl-carbonylaminoacetic acid 2. Various aldehydes on treatment with compound 2 in acetic anhydride to gave 1,3-oxazol-5-ones