Cas 163705-83-7,2-((R)-1-Phenyl-ethylamino)-cyclopent-1-enecarboxylic acid ethyl ester

163705-83-7

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Basic information

Product Name: 2-((R)-1-Phenyl-ethylamino)-cyclopent-1-enecarboxylic acid ethyl ester
Synonyms: 2-((R)-1-Phenyl-ethylamino)-cyclopent-1-enecarboxylic acid ethyl ester
CAS NO:163705-83-7
Molecular Formula:
Molecular Weight: 259.348
EINECS: N/A
Product Categories: N/A
Mol File: 163705-83-7.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-((R)-1-Phenyl-ethylamino)-cyclopent-1-enecarboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-((R)-1-Phenyl-ethylamino)-cyclopent-1-enecarboxylic acid ethyl ester(163705-83-7)
EPA Substance Registry System: 2-((R)-1-Phenyl-ethylamino)-cyclopent-1-enecarboxylic acid ethyl ester(163705-83-7)

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: 163705-83-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 163705-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,7,0 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 163705-83:
(8*1)+(7*6)+(6*3)+(5*7)+(4*0)+(3*5)+(2*8)+(1*3)=137
137 % 10 = 7
So 163705-83-7 is a valid CAS Registry Number.

163705-83-7Upstream product

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163705-83-7Relevant articles and documents

Asymmetric formation of quaternary centers through aza-annulation of chiral β-enamino esters with acrylate derivatives

Barta, Nancy S.,Brode, Adam,Stille, John R.

, p. 6201 - 6206 (2007/10/02)

The aza-annulation of β-enamino ester substrates with acrylate derivatives was used for the stereoselective formation of quaternary carbon centers. Tetrasubstituted secondary enamines, in which the enamine tautomer was stabilized through conjugation with

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