1311291-88-9 Usage
Uses
Used in Organic Synthesis:
[1,1'-Biphenyl]-4-carboxylic acid, 3'-(bromoMethyl)-, Methyl ester is used as a building block in the synthesis of various biologically active molecules. Its bromoMethyl group allows for the introduction of functional groups into organic molecules, making it a versatile compound for creating diverse chemical structures.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, [1,1'-Biphenyl]-4-carboxylic acid, 3'-(bromoMethyl)-, Methyl ester is used as a reagent in organic reactions, contributing to the development of new drugs and therapeutic agents.
Used in Medicinal Chemistry:
[1,1'-Biphenyl]-4-carboxylic acid, 3'-(broMoMethyl)-, Methyl ester has potential applications in medicinal chemistry due to its unique chemical properties, which can be exploited to design and synthesize novel pharmaceutical compounds with specific biological activities.
Used in Material Science:
[1,1'-Biphenyl]-4-carboxylic acid, 3'-(bromoMethyl)-, Methyl ester's structural features make it a useful scaffold for creating materials with specific properties, such as those used in the development of advanced materials for various applications in material science.
Check Digit Verification of cas no
The CAS Registry Mumber 1311291-88-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,1,2,9 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1311291-88:
(9*1)+(8*3)+(7*1)+(6*1)+(5*2)+(4*9)+(3*1)+(2*8)+(1*8)=119
119 % 10 = 9
So 1311291-88-9 is a valid CAS Registry Number.
1311291-88-9Relevant academic research and scientific papers
Modular assembly of macrocyclic organo-peptide hybrids using synthetic and genetically encoded precursors
Smith, Jessica M.,Vitali, Francesca,Archer, Steven A.,Fasan, Rudi
, p. 5075 - 5080 (2011/06/28)
Mix, click, cyclize: Conformationally constrained organo-peptide hybrids can be constructed by a tandem chemoselective reaction between a synthetic molecule and a recombinant protein. Diverse macrocyclic structures were obtained in cyclic, lariat, and protein-tethered configurations by varying the nature of the synthetic and biosynthetic precursors. Copyright
