Cas 1443224-48-3,tert-butyl ((1S)-2-{[(1S)-1-benzyl-3,3-dicyano-2-hydroxyprop-2-en-1-yl]amino}-1-methyl-2-oxoethyl)carbamate

1443224-48-3

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Basic information

Product Name: tert-butyl ((1S)-2-{[(1S)-1-benzyl-3,3-dicyano-2-hydroxyprop-2-en-1-yl]amino}-1-methyl-2-oxoethyl)carbamate
Synonyms: tert-butyl ((1S)-2-{[(1S)-1-benzyl-3,3-dicyano-2-hydroxyprop-2-en-1-yl]amino}-1-methyl-2-oxoethyl)carbamate
CAS NO:1443224-48-3
Molecular Formula:
Molecular Weight: 384.435
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: tert-butyl ((1S)-2-{[(1S)-1-benzyl-3,3-dicyano-2-hydroxyprop-2-en-1-yl]amino}-1-methyl-2-oxoethyl)carbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl ((1S)-2-{[(1S)-1-benzyl-3,3-dicyano-2-hydroxyprop-2-en-1-yl]amino}-1-methyl-2-oxoethyl)carbamate(1443224-48-3)
EPA Substance Registry System: tert-butyl ((1S)-2-{[(1S)-1-benzyl-3,3-dicyano-2-hydroxyprop-2-en-1-yl]amino}-1-methyl-2-oxoethyl)carbamate(1443224-48-3)

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: 1443224-48-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1443224-48-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,3,2,2 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1443224-48:
(9*1)+(8*4)+(7*4)+(6*3)+(5*2)+(4*2)+(3*4)+(2*4)+(1*8)=133
133 % 10 = 3
So 1443224-48-3 is a valid CAS Registry Number.

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1443224-48-3Relevant academic research and scientific papers

Peptidoyl benzotriazolide-mediated acylation of nitrile-activated methylene groups

Sahu, Sandhyamayee,Lebedyeva, Iryna O.,Panda, Siva S.,Katritzky, Alan R.

, p. 1256 - 1260 (2013)

Peptidoyl benzotriazoles permit the acylation of active methylene groups of nitriles to provide CH-acylated nitrile enols from α-amino acids or from di- or tripeptides with no loss of chirality. Georg Thieme Verlag Stuttgart.New York.

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