Cas 1314778-07-8,(S,Z)-benzyl 3-tert-butoxy-1-(1-hydroxybut-2-en-2-ylamino)-1-oxopropan-2-ylcarbamate

1314778-07-8

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Basic information

Product Name: (S,Z)-benzyl 3-tert-butoxy-1-(1-hydroxybut-2-en-2-ylamino)-1-oxopropan-2-ylcarbamate
Synonyms: (S,Z)-benzyl 3-tert-butoxy-1-(1-hydroxybut-2-en-2-ylamino)-1-oxopropan-2-ylcarbamate
CAS NO:1314778-07-8
Molecular Formula:
Molecular Weight: 364.442
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,Z)-benzyl 3-tert-butoxy-1-(1-hydroxybut-2-en-2-ylamino)-1-oxopropan-2-ylcarbamate(CAS DataBase Reference)
NIST Chemistry Reference: (S,Z)-benzyl 3-tert-butoxy-1-(1-hydroxybut-2-en-2-ylamino)-1-oxopropan-2-ylcarbamate(1314778-07-8)
EPA Substance Registry System: (S,Z)-benzyl 3-tert-butoxy-1-(1-hydroxybut-2-en-2-ylamino)-1-oxopropan-2-ylcarbamate(1314778-07-8)

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: 1314778-07-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1314778-07-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,7,7 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1314778-07:
(9*1)+(8*3)+(7*1)+(6*4)+(5*7)+(4*7)+(3*8)+(2*0)+(1*7)=158
158 % 10 = 8
So 1314778-07-8 is a valid CAS Registry Number.

1314778-07-8Upstream product

1314778-07-8Downstream Products

1314778-08-9 (S,Z)-benzyl 3-tert-butoxy-1-(methyl(1-tritylthiobut-2-en-2-yl)amino)-1-oxopropan-2-ylcarbamate

1314778-07-8Relevant academic research and scientific papers

Fmoc synthesis of peptide thioesters without post-chain-assembly manipulation

Zheng, Ji-Shen,Chang, Hao-Nan,Wang, Feng-Liang,Liu, Lei

supporting information; experimental part, p. 11080 - 11083 (2011/09/15)

An operationally simple method for the synthesis of peptide thioesters is developed using standard Fmoc solid-phase peptide synthesis procedures. The method relies on the use of a premade enamide-containing amino acid which, in the final TFA cleavage step

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