150700-52-0 Usage
Uses
Used in Pharmaceutical Synthesis:
+-/-4-Chlor-benzhydrylamine (Racem) is used as a key intermediate in the pharmaceutical industry for the synthesis of various drug molecules. Its chiral amine structure allows for the creation of enantiomerically pure compounds, which are crucial for the development of effective and safe medications.
Used in Organic Chemistry Reactions:
In the field of organic chemistry, +-/-4-Chlor-benzhydrylamine (Racem) is utilized as a reagent, particularly in the preparation of chiral compounds. Its ability to participate in asymmetric synthesis makes it a valuable tool for creating enantiomerically enriched products, which are essential for various applications in the chemical industry.
Used in Asymmetric Synthesis:
+-/-4-Chlor-benzhydrylamine (Racem) is employed as a starting material in asymmetric synthesis, a technique that allows for the selective production of one enantiomer over the other. This is particularly important in the development of pharmaceuticals, as the different enantiomers of a compound can have significantly different biological activities and effects.
Used in Chemical Compound Production:
+-/-4-Chlor-benzhydrylamine (Racem) serves as an important building block for the production of various chemical compounds. Its unique structure and reactivity make it a versatile component in the synthesis of a wide range of molecules, contributing to the advancement of the chemical industry and the development of new materials and products.
Check Digit Verification of cas no
The CAS Registry Mumber 150700-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,7,0 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 150700-52:
(8*1)+(7*5)+(6*0)+(5*7)+(4*0)+(3*0)+(2*5)+(1*2)=90
90 % 10 = 0
So 150700-52-0 is a valid CAS Registry Number.
150700-52-0Relevant articles and documents
Enantioselective Hydrogenation of Diarylmethanimines for Synthesis of Chiral Diarylmethylamines
Kong, Duanyang,Li, Meina,Zi, Guofu,Hou, Guohua,He, Yong
, p. 6640 - 6648 (2016)
An enantioselective hydrogenation of N-substituted diarylmethanimines under mild conditions has been first realized by using an iridium catalyst with a chiral f-spiroPhos ligand. This method provides an efficient access to the asymmetric synthesis of a variety of chiral diarylmethylamines and their derivatives with excellent enantioselectivities (up to 99.4% ee) and high turnover numbers (TON up to 4000).
