123436-11-3 Usage
Uses
Used in Pharmaceutical Research:
(-)-(3-bromophenyl)phenylmethanol is used as a building block for the production of various pharmaceuticals. Its unique stereochemistry allows for the development of enantiomerically pure compounds, which can have different biological activities and reduce potential side effects.
Used in Agrochemical Production:
(-)-(3-bromophenyl)phenylmethanol is used as a precursor in the production of agrochemicals, contributing to the development of effective and targeted pesticides and other agricultural products.
Used in Organic Synthesis:
(-)-(3-bromophenyl)phenylmethanol is used as a key intermediate in the synthesis of biologically active compounds and fine chemicals, enabling the creation of new and improved molecules for various applications.
Used in Asymmetric Synthesis and Chiral Catalysis Research:
(-)-(3-bromophenyl)phenylmethanol is used as a valuable tool for studying asymmetric synthesis and chiral catalysis, helping to advance the understanding of stereoselective reactions and the development of enantioselective catalysts.
Check Digit Verification of cas no
The CAS Registry Mumber 123436-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,4,3 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 123436-11:
(8*1)+(7*2)+(6*3)+(5*4)+(4*3)+(3*6)+(2*1)+(1*1)=93
93 % 10 = 3
So 123436-11-3 is a valid CAS Registry Number.
123436-11-3Relevant articles and documents
Enantioselective oxidation of diaryl carbinols by Nocardia corallina B-276
Perez, Herminia I.,Luna, Hector,Manjarrez, Norberto,Solis, Aida,Nuez
, p. 4263 - 4268 (2000)
Whole cells of Nocardia corallina B-276 oxidized diaryl carbinols enantioselectively to give ketones in moderate yields, and some of the unreacted alcohols showed high ee's. This asymmetric oxidation is a simple and efficient method for preparing meta- and para-monosubstituted optically active diaryl carbinols from the racemates. The para-substituted chiral alcohols have an R configuration. (C) 2000 Elsevier Science Ltd.
A NEW PREPARATIVE METHOD FOR OPTICALLY ACTIVE DIARYLCARBINOLS
Toda, Fumio,Tanaka, Koichi,Koshiro, Kenzo
, p. 873 - 874 (2007/10/02)
Some diarylcarbinols were resolved efficiently by complexation with brucine.
