Cas 928259-87-4,4-Pentenoic acid, 2-[(diphenylmethylene)amino]-3-(hydroxymethyl)-, ethyl ester, (3S)-

928259-87-4

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Basic information

Product Name: 4-Pentenoic acid, 2-[(diphenylmethylene)amino]-3-(hydroxymethyl)-, ethyl ester, (3S)-
Synonyms:
CAS NO:928259-87-4
Molecular Formula: C21H23NO3
Molecular Weight: 337.419
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: 4-Pentenoic acid, 2-[(diphenylmethylene)amino]-3-(hydroxymethyl)-, ethyl ester, (3S)-(CAS DataBase Reference)
NIST Chemistry Reference: 4-Pentenoic acid, 2-[(diphenylmethylene)amino]-3-(hydroxymethyl)-, ethyl ester, (3S)-(928259-87-4)
EPA Substance Registry System: 4-Pentenoic acid, 2-[(diphenylmethylene)amino]-3-(hydroxymethyl)-, ethyl ester, (3S)-(928259-87-4)

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: 928259-87-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 928259-87-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,2,5 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 928259-87:
(8*9)+(7*2)+(6*8)+(5*2)+(4*5)+(3*9)+(2*8)+(1*7)=214
214 % 10 = 4
So 928259-87-4 is a valid CAS Registry Number.

928259-87-4Upstream product

928259-87-4Downstream Products

681260-04-8 (1R,2S)-1-amino-2-vinyl-cyclopropyl carboxylic acid methyl ester

928259-87-4Relevant academic research and scientific papers

Catalytic asymmetric synthesis of ethyl (1R,2S)-dehydrocoronamate

Fox, Martin E.,Lennon, Ian C.,Farina, Vittorio

, p. 945 - 948 (2007)

A synthesis of (1R,2S)-dehydrocoronamic acid ethyl ester was developed employing a regio- and enantioselective palladium-catalysed nucleophilic ring-opening of 3,4-epoxy-1-butene with a glycine anion equivalent as the key enantiodifferentiating step. The

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