Cas 115134-33-3,(S)-2-[1-(4-Dimethylamino-phenyl)-2,2-dimethyl-prop-(Z)-ylideneamino]-propionic acid methyl ester

115134-33-3

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Basic information

Product Name: (S)-2-[1-(4-Dimethylamino-phenyl)-2,2-dimethyl-prop-(Z)-ylideneamino]-propionic acid methyl ester
Synonyms: (S)-2-[1-(4-Dimethylamino-phenyl)-2,2-dimethyl-prop-(Z)-ylideneamino]-propionic acid methyl ester
CAS NO:115134-33-3
Molecular Formula:
Molecular Weight: 290.406
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: (S)-2-[1-(4-Dimethylamino-phenyl)-2,2-dimethyl-prop-(Z)-ylideneamino]-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-[1-(4-Dimethylamino-phenyl)-2,2-dimethyl-prop-(Z)-ylideneamino]-propionic acid methyl ester(115134-33-3)
EPA Substance Registry System: (S)-2-[1-(4-Dimethylamino-phenyl)-2,2-dimethyl-prop-(Z)-ylideneamino]-propionic acid methyl ester(115134-33-3)

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: 115134-33-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 115134-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,1,3 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115134-33:
(8*1)+(7*1)+(6*5)+(5*1)+(4*3)+(3*4)+(2*3)+(1*3)=83
83 % 10 = 3
So 115134-33-3 is a valid CAS Registry Number.

115134-33-3Upstream product

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115134-33-3Relevant academic research and scientific papers

ENANTIOSELECTIVE METHYLATION OF GLYCINE INFLUENCE OF THE STRUCTURE OF THE CHIRAL NUCLEOFUGAL

Duhamel, Pierre,Eddine, Jamal Jamal,Valnot, Jean-Yves

, p. 3801 - 3804 (1987)

Variation of the enantioselection from e.e.= 0 to 76percent was observed in the enantioface differentiation of the prochiral enolates 2a and 2b by a serie of mixed sulfates derived from D-(+)-glucose.

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