320385-10-2 Usage
Uses
Used in Pharmaceutical Industry:
(E)-3-benzyloxypropenoyl-(2'S)-bornane-10,2-sultam is used as a compound of interest for its potential pharmaceutical applications due to its unique structure and properties. (E)-3-benzyloxypropenoyl-(2'S)-bornane-10,2-sultam's ability to interact with biological targets and its potential for drug development make it a valuable candidate for further research and exploration.
Used in Drug Development:
In the field of drug development, (E)-3-benzyloxypropenoyl-(2'S)-bornane-10,2-sultam is used as a starting point for the design and synthesis of new therapeutic agents. Its unique molecular architecture may provide insights into novel mechanisms of action and help in the development of more effective treatments for various diseases and conditions.
Used in Research and Development:
(E)-3-benzyloxypropenoyl-(2'S)-bornane-10,2-sultam is also used as a research tool to study its biological activities and potential interactions with biological systems. This can lead to a better understanding of the compound's properties and its potential applications in various fields, including medicine, biology, and chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 320385-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,0,3,8 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 320385-10:
(8*3)+(7*2)+(6*0)+(5*3)+(4*8)+(3*5)+(2*1)+(1*0)=102
102 % 10 = 2
So 320385-10-2 is a valid CAS Registry Number.
320385-10-2Relevant academic research and scientific papers
Process for the preparation of substituted pyrrolidine derivatives and intermediates
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Page/Page column 7-8, (2010/11/08)
Two syntheses are provided; one for the preparation of (3R,4R)-4-(hydroxymethyl)pyrrolidin-3-ol, and other for the preparation of (3S,4R)-4-(hydroxymethyl)pyrrolidin-3-ol. (3R,4R)-4-(hydroxymethyl)pyrrolidin-3-ol is prepared using the achiral ylide prepared from benzylamine instead of phenethylamine (Scheme 3) which provides a crystalline intermediate. The synthesis of (3S,4R)-4-(hydroxymethyl)pyrrolidin-3-ol is achieved from (S)-diethylmalate as described in Scheme 4. A process for preparing camphor sultam is also provided.
A practical large-scale synthesis of (3R,4R)-4-(Hydroxymethyl)pyrrolidin-3- ol via asymmetric 1,3-dipolar cycloaddition
Kotian, Pravin L.,Lin, Tsu-Hsing,El-Kattan, Yahya,Chand, Pooran
, p. 193 - 197 (2012/12/24)
(3R,4R)-4-(Hydroxymethyl)pyrrolidin-3-ol (1), which is a useful intermediate for the synthesis of various bioactive molecules, has been synthesized in 51% overall yield by 1,3-dipolar cycloaddition reaction from the dipolarophile, (E)-3-benzyloxypropenoyl-(2′S)-bornane-10,2-sultam (5), and the achiral ylide precursor, N-(benzyl)-N-(methoxymethyl)-N- (trimethylsilylmethyl)amine (6), without using chromatography and the subsequent reduction with LAH and catalytic hydrogenation. The diastereomers 7 and 8 were separated by crystallization, and efficient procedures were developed for the subsequent reactions to afford 1.
