137090-44-9 Usage
Description
CHEMBRDG-BB 4013762, with the molecular formula C9H14N2O3S, is an amide derivative and a heterocyclic compound. It is a chemical compound used in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceutical products. Its unique chemical properties and potential pharmacological activities make it a valuable ingredient in the production of therapeutic agents and an important compound in the field of medicinal chemistry.
Uses
Used in Pharmaceutical Industry:
CHEMBRDG-BB 4013762 is used as a building block for the synthesis of various drugs and pharmaceutical products. Its unique chemical properties and potential pharmacological activities make it a valuable ingredient in the development of therapeutic agents.
Used in Drug Discovery and Development:
CHEMBRDG-BB 4013762 is utilized in drug discovery and development processes due to its potential pharmacological activities. It serves as a key component in the creation of new drugs and pharmaceutical products, contributing to advancements in medicinal chemistry.
Used in Study of Biological Activities and Interactions:
CHEMBRDG-BB 4013762 is studied for its biological activities and interactions, making it an important compound in the field of medicinal chemistry. Understanding its interactions with biological systems can lead to the development of more effective and targeted therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 137090-44-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,0,9 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 137090-44:
(8*1)+(7*3)+(6*7)+(5*0)+(4*9)+(3*0)+(2*4)+(1*4)=119
119 % 10 = 9
So 137090-44-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H12ClNO/c1-8-3-5-10(6-4-8)12-14-11(7-13)9(2)15-12/h3-6H,7H2,1-2H3
137090-44-9Relevant articles and documents
1,3-Oxazole-isoniazid hybrids: Synthesis, antitubercular activity, and their docking studies
Katariya, Kanubhai D.,Shah, Shailesh R.
, (2020/01/25)
A series of novel N′-([2-aryl-5-methyl-1,3-oxazole-4-yl]methylene)isonicotino/nicotino hydrazides 10a-l were prepared by the condensation reaction of 2-aryl-5-methyl-1,3-oxazole-4-carbaldehydes 8a-f with the corresponding isonicotino/nicotino hydrazides 9
SUBSTITUTED ACID DERIVATIVES USEFUL AS ANTIDIABETIC AND ANTIOBESITY AGENTS AND METHOD
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Page/Page column 29, (2010/11/29)
Compounds are provided which have the structure of Formula (I): wherein R is hydrogen or C1-C4 alkyl; and each of R1 and R2 is independently hydrogen, C1-C4 alkyl, halo or C1-Cs
METHOD FOR THE PRODUCTION OF OXAZOLES BY CONDENSING AROMATIC ALDEHYDES WITH A-KETOXIMES TO N-OXIDES AND THEN REACTING THE SAME WITH ACTIVATED ACID DERIVATIVES
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Page/Page column 18, (2008/06/13)
Disclosed is a method for producing oxazoles of formula IV by condensing aromatic aldehydes with a-ketoximes to N-oxides and then reacting the same with activated acid derivatives. The invention relates to a method for producing oxazoles by condensing ald