31161-47-4 Usage
Description
(3-Bromophenyl)(2-thienyl)Methanone, also known as 2-(3-bromophenyl)thiophen-3-ylmethanone, is a chemical compound with the molecular formula C14H9BrOS. It is a ketone compound that contains a bromophenyl group and a thienyl group. This chemical is commonly used as an intermediate in organic synthesis and pharmaceutical research. It has also been studied for its potential applications in the development of new drugs and other biologically active compounds. As a ketone, (3-Bromophenyl)(2-thienyl)Methanone possesses carbonyl functionality, making it a versatile building block for the creation of diverse organic molecules with various properties and applications.
Uses
Used in Organic Synthesis:
(3-Bromophenyl)(2-thienyl)Methanone is used as an intermediate in organic synthesis for the creation of diverse organic molecules with various properties and applications.
Used in Pharmaceutical Research:
(3-Bromophenyl)(2-thienyl)Methanone is used as a building block in pharmaceutical research for the development of new drugs and other biologically active compounds.
Used in Drug Development:
(3-Bromophenyl)(2-thienyl)Methanone is used in the development of new drugs and other biologically active compounds due to its potential applications in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 31161-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,6 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 31161-47:
(7*3)+(6*1)+(5*1)+(4*6)+(3*1)+(2*4)+(1*7)=74
74 % 10 = 4
So 31161-47-4 is a valid CAS Registry Number.
31161-47-4Relevant articles and documents
Catalytic asymmetric alkylation of aryl heteroaryl ketones
Ortiz, Pablo,Del Hoyo, Ana M.,Harutyunyan, Syuzanna R.
supporting information, p. 72 - 76 (2015/02/19)
Tertiary diarylmethanols are highly bioactive structural motifs. A new strategy to access chiral tertiary diarylmethanols through copper-catalyzed direct alkylation of (di)(hetero)aryl ketones by using Grignard reagents was developed. The low reactivity a