Cas 1192024-61-5,(S)-benzyl 2-((S)-(tert-butoxycarbonylamino)(p-tolyl)-methyl)-2-fluoro-3-oxobutanoate

1192024-61-5

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Basic information

Product Name: (S)-benzyl 2-((S)-(tert-butoxycarbonylamino)(p-tolyl)-methyl)-2-fluoro-3-oxobutanoate
Synonyms: (S)-benzyl 2-((S)-(tert-butoxycarbonylamino)(p-tolyl)-methyl)-2-fluoro-3-oxobutanoate
CAS NO:1192024-61-5
Molecular Formula:
Molecular Weight: 429.488
EINECS: N/A
Product Categories: N/A
Mol File: 1192024-61-5.mol
Article Data: 2

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)-benzyl 2-((S)-(tert-butoxycarbonylamino)(p-tolyl)-methyl)-2-fluoro-3-oxobutanoate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-benzyl 2-((S)-(tert-butoxycarbonylamino)(p-tolyl)-methyl)-2-fluoro-3-oxobutanoate(1192024-61-5)
EPA Substance Registry System: (S)-benzyl 2-((S)-(tert-butoxycarbonylamino)(p-tolyl)-methyl)-2-fluoro-3-oxobutanoate(1192024-61-5)

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: 1192024-61-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1192024-61-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,0,2 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1192024-61:
(9*1)+(8*1)+(7*9)+(6*2)+(5*0)+(4*2)+(3*4)+(2*6)+(1*1)=125
125 % 10 = 5
So 1192024-61-5 is a valid CAS Registry Number.

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1192024-61-5Relevant articles and documents

Asymmetric mannich-type reactions of fluorinated ketoesters with binaphthyl-modified thiourea catalysts

Kang, Young Ku,Yoon, Sung Je,Kim, Dae Young

experimental part, p. 1195 - 1200 (2011/11/06)

The catalytic enantioselective Mannich-type reaction promoted by chiral binaphthyl-modified bifunctional organocatalysts is described. The treatment of α-fluoro-β-ketoesters with N-Boc imines under mild reaction conditions afforded the corresponding β-aminated α-fluoro-β- ketoesters with excellent enantioselectivities (up to 98% ee).

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