157635-94-4 Usage
Molecular weight
353.4
Structure
A complex structure that includes a piperidine ring and an ester group
Chirality
A chiral compound with a specific stereochemistry designated as (R)-, indicating the specific three-dimensional arrangement of the molecule's atoms
Functional groups
Acetyloxy group, hydroxymethyl group, and a phenylmethyl ester group
Pharmacological applications
Potential pharmaceutical applications due to its structural features, including the acetyloxy and hydroxymethyl groups, which can interact with biological systems and potentially exhibit pharmacological activity. The phenylmethyl ester group also contributes to its potential pharmacological properties.
Research and development
The compound's specific stereochemistry and complex structure make it an interesting target for pharmacological research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 157635-94-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,6,3 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 157635-94:
(8*1)+(7*5)+(6*7)+(5*6)+(4*3)+(3*5)+(2*9)+(1*4)=164
164 % 10 = 4
So 157635-94-4 is a valid CAS Registry Number.
157635-94-4Relevant academic research and scientific papers
Enzymatic preparation of homochiral 2-(N-carbobenzyloxypiperid-4-yl)-1,3-propanediol monoacetate. A facile entry to both enantiomers of 3-hydroxymethylquinuclidine
Guanti,Banfi,Brusco,Narisano
, p. 537 - 540 (2007/10/02)
Both enantiomers of monoacetate 1 have been prepared in high ee by lipase catalyzed monohydrolysis of the prochiral diacetate 3 and by monoacetylation of the corresponding diol 4.3-Hydroxymethylquinuclidine 2 was then synthesized in both enantiomeric form
