Cas 1000677-22-4,tert-butyl (S)-1-[(S)-1-(hydroxycarbamoyl)-2-phenylethylcarbamoyl]-2-methylpropylcarbamate

1000677-22-4

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Basic information

Product Name: tert-butyl (S)-1-[(S)-1-(hydroxycarbamoyl)-2-phenylethylcarbamoyl]-2-methylpropylcarbamate
Synonyms: tert-butyl (S)-1-[(S)-1-(hydroxycarbamoyl)-2-phenylethylcarbamoyl]-2-methylpropylcarbamate
CAS NO:1000677-22-4
Molecular Formula:
Molecular Weight: 379.456
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 (S)-1-[(S)-1-(hydroxycarbamoyl)-2-phenylethylcarbamoyl]-2-methylpropylcarbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (S)-1-[(S)-1-(hydroxycarbamoyl)-2-phenylethylcarbamoyl]-2-methylpropylcarbamate(1000677-22-4)
EPA Substance Registry System: tert-butyl (S)-1-[(S)-1-(hydroxycarbamoyl)-2-phenylethylcarbamoyl]-2-methylpropylcarbamate(1000677-22-4)

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: 1000677-22-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1000677-22-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,6,7 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1000677-22:
(9*1)+(8*0)+(7*0)+(6*0)+(5*6)+(4*7)+(3*7)+(2*2)+(1*2)=94
94 % 10 = 4
So 1000677-22-4 is a valid CAS Registry Number.

1000677-22-4Upstream product

20902-47-0 N-tert-butoxycarbonyl-L-valyl-L-phenylalanine methyl ester

1000677-22-4Downstream Products

1000677-22-4Relevant academic research and scientific papers

Microwave-assisted transformation of esters into hydroxamic acids

Massaro, Assunta,Mordini, Alessandro,Reginato, Gianna,Russo, Francesco,Taddei, Maurizio

, p. 3201 - 3204 (2008/09/16)

A general, mild and efficient procedure with which to access hydroxamic acids, in good yields and purity, is reported. Esters are used as substrates and reacted with hydroxylamine, in the presence of a base, under microwave activation. The method has been

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