Cas 1100357-19-4,(R,Z)-tert-butyl 4-(2-(benzyloxycarbonylamino)-3-methoxy-3-oxoprop-1-enyl)-2,2,4-trimethyloxazolidine-3-carboxylate

1100357-19-4

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Basic information

Product Name: (R,Z)-tert-butyl 4-(2-(benzyloxycarbonylamino)-3-methoxy-3-oxoprop-1-enyl)-2,2,4-trimethyloxazolidine-3-carboxylate
Synonyms: (R,Z)-tert-butyl 4-(2-(benzyloxycarbonylamino)-3-methoxy-3-oxoprop-1-enyl)-2,2,4-trimethyloxazolidine-3-carboxylate
CAS NO:1100357-19-4
Molecular Formula:
Molecular Weight: 448.516
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: (R,Z)-tert-butyl 4-(2-(benzyloxycarbonylamino)-3-methoxy-3-oxoprop-1-enyl)-2,2,4-trimethyloxazolidine-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (R,Z)-tert-butyl 4-(2-(benzyloxycarbonylamino)-3-methoxy-3-oxoprop-1-enyl)-2,2,4-trimethyloxazolidine-3-carboxylate(1100357-19-4)
EPA Substance Registry System: (R,Z)-tert-butyl 4-(2-(benzyloxycarbonylamino)-3-methoxy-3-oxoprop-1-enyl)-2,2,4-trimethyloxazolidine-3-carboxylate(1100357-19-4)

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: 1100357-19-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1100357-19-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,0,3,5 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1100357-19:
(9*1)+(8*1)+(7*0)+(6*0)+(5*3)+(4*5)+(3*7)+(2*1)+(1*9)=84
84 % 10 = 4
So 1100357-19-4 is a valid CAS Registry Number.

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1100357-19-4Relevant academic research and scientific papers

Short and stereoselective synthesis of manzacidins A and C, and their enantiomers

Oe, Kentaro,Shinada, Tetsuro,Ohfune, Yasufumi

, p. 7426 - 7429 (2008)

A short and stereoselective synthesis of manzacidins A and C, and their enantiomers was achieved via stereoselective hydrogenation reactions of dehydroamino acid esters 5-8 using a chiral Rh catalyst.

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