Cas 107326-52-3,2-[Bis-(3-methyl-but-3-enyl)-amino]-3-phenyl-propionic acid methyl ester

107326-52-3

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Basic information

Product Name: 2-[Bis-(3-methyl-but-3-enyl)-amino]-3-phenyl-propionic acid methyl ester
Synonyms:
CAS NO:107326-52-3
Molecular Formula:
Molecular Weight: 315.456
EINECS: N/A
Product Categories: N/A
Mol File: 107326-52-3.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: 2-[Bis-(3-methyl-but-3-enyl)-amino]-3-phenyl-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[Bis-(3-methyl-but-3-enyl)-amino]-3-phenyl-propionic acid methyl ester(107326-52-3)
EPA Substance Registry System: 2-[Bis-(3-methyl-but-3-enyl)-amino]-3-phenyl-propionic acid methyl ester(107326-52-3)

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: 107326-52-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 107326-52-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,3,2 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 107326-52:
(8*1)+(7*0)+(6*7)+(5*3)+(4*2)+(3*6)+(2*5)+(1*2)=103
103 % 10 = 3
So 107326-52-3 is a valid CAS Registry Number.

107326-52-3Upstream product

107326-52-3Downstream Products

107326-52-3Relevant articles and documents

Reactions of Allystannanes with in Situ Generated Immonium Salts in Protic Solvent: A Facile Aminomethano Destannylation Process

Grieco, Paul A.,Bahsas, Ali

, p. 1378 - 1380 (2007/10/02)

In situ generated immoniunm salts derived from primary amines and formaldehyde upon exposure to allylstannanes in protic media undergo rapid, facile aminomethano destannylation, giving rise to bishomoallylamines with no evidence of piperidine formation.

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