Cas 125285-04-3,Diisopropyl-carbamic acid (E)-(R)-1-((S)-1-benzyloxy-ethyl)-2-oxo-pent-3-enyl ester

125285-04-3

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Basic information

Product Name: Diisopropyl-carbamic acid (E)-(R)-1-((S)-1-benzyloxy-ethyl)-2-oxo-pent-3-enyl ester
Synonyms:
CAS NO:125285-04-3
Molecular Formula:
Molecular Weight: 361.481
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: Diisopropyl-carbamic acid (E)-(R)-1-((S)-1-benzyloxy-ethyl)-2-oxo-pent-3-enyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Diisopropyl-carbamic acid (E)-(R)-1-((S)-1-benzyloxy-ethyl)-2-oxo-pent-3-enyl ester(125285-04-3)
EPA Substance Registry System: Diisopropyl-carbamic acid (E)-(R)-1-((S)-1-benzyloxy-ethyl)-2-oxo-pent-3-enyl ester(125285-04-3)

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: 125285-04-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 125285-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,2,8 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 125285-04:
(8*1)+(7*2)+(6*5)+(5*2)+(4*8)+(3*5)+(2*0)+(1*4)=113
113 % 10 = 3
So 125285-04-3 is a valid CAS Registry Number.

125285-04-3Upstream product

125285-04-3Downstream Products

125285-04-3Relevant academic research and scientific papers

ENANTIOMERICALLY PURE α',β'-DIFUNCTIONALIZED α,β-ENONES BY HIGHLY DIASTEREOSELECTIVE NUCLEOPHILIC ALKENOYLATION OF CHIRAL ALDEHYDES

Tebben, Petra,Reggelin, Michael,Hoppe, Dieter

, p. 2919 - 2922 (2007/10/02)

The nucleophilic alkenoylation of protected chiral α-oxy and α-amino alkanals 3 by lithiated 1-(p-toluenesulfonyl)-2-alkenyl carbamates 2 proceeds with virtually complete stereoselectivity to form the syn-diastereoisomers of the title compounds 4.

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