Cas 936229-53-7,3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid benzyl ester

936229-53-7

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Basic information

Product Name: 3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid benzyl ester
Synonyms: 3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid benzyl ester
CAS NO:936229-53-7
Molecular Formula:
Molecular Weight: 313.784
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid benzyl ester(936229-53-7)
EPA Substance Registry System: 3-(4-chloro-phenyl)-2,3-dihydro-pyrrole-1-carboxylic acid benzyl ester(936229-53-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 936229-53-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 936229-53-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,6,2,2 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 936229-53:
(8*9)+(7*3)+(6*6)+(5*2)+(4*2)+(3*9)+(2*5)+(1*3)=187
187 % 10 = 7
So 936229-53-7 is a valid CAS Registry Number.

936229-53-7Upstream product

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936229-53-7Relevant academic research and scientific papers

Synthesis of conformationally restricted acetylcholine analogues. Comparing lipase-mediated resolution with simulated moving bed chromatography of arylated β-hydroxy-pyrrolidines

Barreto, Ricardo de L.,Carpes, Marcos J.S.,Santana, Cesar C.,Correia, Carlos R.D.

, p. 435 - 442 (2007)

The enantiodivergent synthesis of new, conformationally restricted acetylcholine analogues was accomplished using arylated endocyclic enecarbamates as key intermediates. Stereoselective hydroboration of the aryl enecarbamates provided the corresponding ar

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