860771-95-5 Usage
Uses
Used in Pharmaceutical Industry:
(3-bromo-phenyl)-hydroxy-acetic acid methyl ester is used as a key intermediate in the synthesis of new drugs, contributing to the development of novel pharmaceuticals with potential therapeutic applications. Its unique structure allows for the creation of diverse chemical entities that can target specific biological pathways or receptors.
Used in Agrochemical Industry:
In the agrochemical sector, (3-bromo-phenyl)-hydroxy-acetic acid methyl ester is utilized as a starting material for the production of various agrochemicals, such as pesticides and herbicides. Its structural properties enable the design of effective compounds that can protect crops from pests and enhance agricultural productivity.
Used in Materials Science:
(3-bromo-phenyl)-hydroxy-acetic acid methyl ester also finds applications in materials science, where it can be employed in the development of new materials with specific properties. These materials may have potential uses in various industries, such as electronics, automotive, and aerospace, where high-performance materials are in demand.
Used in Chemical Research and Development:
(3-bromo-phenyl)-hydroxy-acetic acid methyl ester is also valuable in the field of chemical research and development, where it can be used to explore new chemical reactions and processes. This can lead to the discovery of innovative synthetic methods and the creation of new compounds with unique properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 860771-95-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,0,7,7 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 860771-95:
(8*8)+(7*6)+(6*0)+(5*7)+(4*7)+(3*1)+(2*9)+(1*5)=195
195 % 10 = 5
So 860771-95-5 is a valid CAS Registry Number.
860771-95-5Relevant academic research and scientific papers
Kinetic resolution of mandelate esters via stereoselective acylation catalyzed by lipase PS-30
Chen, Peiran,Yang, Wenhong
, p. 2290 - 2294 (2014/04/17)
By using lipase PS-30 as catalyst, the kinetic resolution of a series of racemic mandelate esters has been achieved via stereoselective acylation. The value of kinetic enantiomeric ratio (E) reached up to 197.5. Substituent effect is briefly discussed.
Synthesis and cannabinoid-1 receptor binding affinity of conformationally constrained analogs of taranabant
Kopka, Ihor E.,Lin, Linus S.,Jewell, James P.,Lanza, Thomas J.,Fong, Tung M.,Shen, Chun-Pyn,Lao, Zhege J.,Ha, Sookhee,Castonguay, Laurie G.,Van Der Ploeg, Lex,Goulet, Mark T.,Hagmann, William K.
scheme or table, p. 4757 - 4761 (2010/10/02)
The design, synthesis, and binding activity of ring constrained analogs of the acyclic cannabinoid-1 receptor (CB1R) inverse agonist taranabant 1 are described. The initial inspiration for these taranabant derivatives was its conformation 1a, determined b
Chiral β-diketonate ligands of 'pseudo planar chiral' topology: Enantioselective synthesis and transition metal complexation
Bocknack, Brian M.,Wang, Long-Cheng,Hughes, Freddie W.,Krische, Michael J.
, p. 6266 - 6275 (2007/10/03)
A practical enantioselective synthesis of chiral β-diketonate ligands 1a-1d, which are of 'pseudo planar-chiral' topology, is described. Additionally, the first chiral bis(diketonates) 2a-2c, ligands of C2-symmetry that are isoelectronic with r
