116174-40-4 Usage
Uses
Used in Organic Synthesis:
Cyclohexanecarboxamide, 2-(hydroxymethyl)-, (1S-trans)(9CI) is used as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure allows for the formation of new molecules with potential applications in different industries.
Used in Pharmaceutical Production:
Cyclohexanecarboxamide, 2-(hydroxymethyl)-, (1S-trans)(9CI) is used as an intermediate in the production of pharmaceuticals. Its specific functional groups and configuration enable the development of new drugs with potential therapeutic effects. Cyclohexanecarboxamide, 2-(hydroxymethyl)-, (1S-trans)(9CI)'s properties may contribute to the discovery of novel medications for various medical conditions.
Used in Chemical Research:
Cyclohexanecarboxamide, 2-(hydroxymethyl)-, (1S-trans)(9CI) is utilized in chemical research to study the properties and reactions of cyclohexanecarboxamide derivatives. Understanding the behavior of Cyclohexanecarboxamide, 2-(hydroxymethyl)-, (1S-trans)- (9CI) can provide insights into the development of new synthetic methods and applications in various fields.
Used in Application Industry:
Cyclohexanecarboxamide, 2-(hydroxymethyl)-, (1S-trans)(9CI) is used as [application type] for [application reason]. (Note: The specific application type and reason are not provided in the materials, so this section cannot be completed without additional information.)
Check Digit Verification of cas no
The CAS Registry Mumber 116174-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,7 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116174-40:
(8*1)+(7*1)+(6*6)+(5*1)+(4*7)+(3*4)+(2*4)+(1*0)=104
104 % 10 = 4
So 116174-40-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO2/c9-8(11)7-4-2-1-3-6(7)5-10/h6-7,10H,1-5H2,(H2,9,11)/t6-,7+/m1/s1
116174-40-4Relevant academic research and scientific papers
Stereoselective synthesis of a trans-octahydroindole derivative, precursor of trandolapril (RU 44 570), an inhibitor of angiotensin converting enzyme
Brion,Marie,Mackiewicz,Roui,Buendia
, p. 4889 - 4892 (2007/10/02)
We describe a stereoselective synthesis of the trans-octahydroindole-2-carboxylic acid 2 a key intermediate in the elaboration of Trandolapril (RU 44 570) 1. The optically active starting material used was obtained by an enzymatic hydrolysis.
