Cas 1393527-61-1,methyl 3-((5-chloro-2-hydroxyphenyl)(1-tosylpyrrolidin-2-yl)methyl)indolizine-1-carboxylate

1393527-61-1

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Basic information

Product Name: methyl 3-((5-chloro-2-hydroxyphenyl)(1-tosylpyrrolidin-2-yl)methyl)indolizine-1-carboxylate
Synonyms: methyl 3-((5-chloro-2-hydroxyphenyl)(1-tosylpyrrolidin-2-yl)methyl)indolizine-1-carboxylate
CAS NO:1393527-61-1
Molecular Formula:
Molecular Weight: 539.052
EINECS: N/A
Product Categories: N/A
Mol File: 1393527-61-1.mol
Article Data: 1

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: methyl 3-((5-chloro-2-hydroxyphenyl)(1-tosylpyrrolidin-2-yl)methyl)indolizine-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 3-((5-chloro-2-hydroxyphenyl)(1-tosylpyrrolidin-2-yl)methyl)indolizine-1-carboxylate(1393527-61-1)
EPA Substance Registry System: methyl 3-((5-chloro-2-hydroxyphenyl)(1-tosylpyrrolidin-2-yl)methyl)indolizine-1-carboxylate(1393527-61-1)

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: 1393527-61-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1393527-61-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,5,2 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1393527-61:
(9*1)+(8*3)+(7*9)+(6*3)+(5*5)+(4*2)+(3*7)+(2*6)+(1*1)=181
181 % 10 = 1
So 1393527-61-1 is a valid CAS Registry Number.

1393527-61-1Upstream product

316375-85-6 methyl indolizine-1-carboxylate

1393527-61-1Downstream Products

1393527-61-1Relevant articles and documents

Palladium(II)-catalyzed enantio- and diastereoselective synthesis of pyrrolidine derivatives

Jana, Ranjan,Pathak, Tejas P.,Jensen, Katrina H.,Sigman, Matthew S.

supporting information; experimental part, p. 4074 - 4077 (2012/09/22)

A palladium-catalyzed enantio- and diastereoselective synthesis of pyrrolidine derivatives is described. Initial intramolecular nucleopalladation of the tethered protected amine forms the pyrrolidine moiety and a quinone methide intermediate. A second nucleophile adds intermolecularly to afford diverse products in high enantio- and diastereoselectivity.

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