112446-73-8 Usage
Uses
Used in Pharmaceutical Industry:
(+)-BETA-CHLORODIISOPINOCAMPHENYLBORANE is used as a reagent for stereoselective reduction reactions in the synthesis of complex organic molecules, which are essential in the development of new pharmaceutical compounds.
Used in Agrochemical Industry:
(+)-BETA-CHLORODIISOPINOCAMPHENYLBORANE is used as a reagent for stereoselective reduction reactions in the synthesis of complex organic molecules, which are crucial in the development of new agrochemical products.
Used in Academic Research Laboratories:
(+)-BETA-CHLORODIISOPINOCAMPHENYLBORANE is used as a reagent for stereoselective reduction reactions in academic research, where chemists explore new synthetic pathways and develop innovative organic molecules for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 112446-73-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,4 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 112446-73:
(8*1)+(7*1)+(6*2)+(5*4)+(4*4)+(3*6)+(2*7)+(1*3)=98
98 % 10 = 8
So 112446-73-8 is a valid CAS Registry Number.
112446-73-8Relevant academic research and scientific papers
THE SYNTHESIS AND REACTIONS OF TRISUBSTITUTED N-(X-2-BENZOTHIAZOLYL)FORMAMIDINES
Lacova, Margita,Nga, Nguyen Thi
, p. 1006 - 1014 (2007/10/02)
The modified Vilsmayer-Haack reagent ANC(O)H-ClSO2C6H5 (A = (CH3)2, (C2H5)2, (CH2)5, CH2CH2OCH2CH2) reacts with 2-amino-X-benzothiazole in pyridine and ether to give three types of products in high yields depending on the character of substituents A and X.Isolated were: N,N-dialkyl-N'-(X-2-benzothiazolyl)formamidines, N,N'-bis(X-2-benzothiazolyl)formamidines, and N,N-dialkyl-N',N''-bis(X-2-benzothiazolyl)triaminomethanes.Investigated were the conditions and reaction products of N,N-dialkyl-N',N''-bis(X-2-benzothiazolyl)triaminomethanes with phenylethanoyl, phenoxyethanoyl, 4-chlorophenoxyethanoyl, and N-phthalimidoethanoyl chloride either in ether or in pyridine.Mutual transformations of the individual products are described.
