135969-66-3 Usage
Uses
Used in Organic Synthesis:
(1S,2R)-2-N-methylaminocyclopentan-1-ol is used as a chiral building block for the synthesis of various organic compounds, providing a specific stereochemistry that is crucial for the desired properties and reactivity of the target molecules.
Used in Pharmaceutical Industry:
(1S,2R)-2-N-methylaminocyclopentan-1-ol is used as an intermediate in the production of pharmaceuticals, where its unique structure and stereochemistry contribute to the development of new drugs with improved efficacy and selectivity.
Used in Chiral Compounds Production:
(1S,2R)-2-N-methylaminocyclopentan-1-ol is used as a precursor for the synthesis of other chiral compounds, which are essential in various industries, including pharmaceuticals, agrochemicals, and fragrances, due to their specific biological activities and enantioselective properties.
Check Digit Verification of cas no
The CAS Registry Mumber 135969-66-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,9,6 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 135969-66:
(8*1)+(7*3)+(6*5)+(5*9)+(4*6)+(3*9)+(2*6)+(1*6)=173
173 % 10 = 3
So 135969-66-3 is a valid CAS Registry Number.
135969-66-3Relevant articles and documents
INDAZOLE COMPOUNDS FOR USE IN TENDON AND/OR LIGAMENT INJURIES
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Page/Page column 62, (2018/04/20)
The present invention provides a compound of formula (I) in free form or in pharmaceutically acceptable salt form (I) a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.
Chemo-enzymatic synthesis of 1,2- and 1,3- amino-alcohols and their use in the enantioselective reduction of acetophenone and anti-acetophenone oxime methyl ether with borane
Didier, Eric,Loubinoux, Bernard,Ramos Tombo, Gerardo H.,Rihs, Grety
, p. 4941 - 4958 (2007/10/02)
New chiral amino-alcohols were enantioselectively synthesized using biotransformations as the key steps. They were used as ligand in the enantioselective borane reduction of acetophenone and of the corresponding anti oxime methyl ether.
