1135292-94-2 Usage
Description
(5-chloro-2-isopropoxyphenyl)methanamine hydrochloride, with a molecular formula of C11H17Cl2NO, is a crystalline solid that appears white to off-white. This chemical compound is widely recognized for its applications in the pharmaceutical industry and chemical research.
Uses
Used in Pharmaceutical Industry:
(5-chloro-2-isopropoxyphenyl)methanamine hydrochloride is used as an intermediate in the synthesis of various drugs. Its unique chemical structure allows it to be a key component in the development of new medications, contributing to the advancement of pharmaceutical treatments.
Used in Organic Synthesis:
In the field of organic synthesis, (5-chloro-2-isopropoxyphenyl)methanamine hydrochloride serves as a valuable reagent. Its versatility in chemical reactions enables the creation of a range of different compounds, expanding the possibilities for chemical innovation and development.
Used in Chemical Research:
As a reagent in chemical research, (5-chloro-2-isopropoxyphenyl)methanamine hydrochloride aids in the exploration of new chemical reactions and the understanding of molecular interactions. Its use in research is crucial for the advancement of scientific knowledge in chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1135292-94-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,5,2,9 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1135292-94:
(9*1)+(8*1)+(7*3)+(6*5)+(5*2)+(4*9)+(3*2)+(2*9)+(1*4)=142
142 % 10 = 2
So 1135292-94-2 is a valid CAS Registry Number.
1135292-94-2Relevant articles and documents
Comparison of different reducing systems in the synthesis of functionally substituted benzylamines from alkyl aryl ketones and aromatic aldehydes
Musatov,Starodubtseva,Turova,Kurilov,Vinogradov,Rakishev,Struchkova
experimental part, p. 1021 - 1028 (2010/11/03)
Different synthetic approaches to functionally substituted benzylamines were examined: reductive amination of alkyl aryl ketones and reduction of aromatic aldehyde oximes. The most efficient procedures were used to prepare a series of previously unknown h
