Cas 928342-25-0,{1-methyl-2-[methyl-(toluene-4-sulfonyl)-amino]-2-oxo-ethyl}-carbamic acid benzyl ester

928342-25-0

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Basic information

Product Name: {1-methyl-2-[methyl-(toluene-4-sulfonyl)-amino]-2-oxo-ethyl}-carbamic acid benzyl ester
Synonyms: {1-methyl-2-[methyl-(toluene-4-sulfonyl)-amino]-2-oxo-ethyl}-carbamic acid benzyl ester
CAS NO:928342-25-0
Molecular Formula:
Molecular Weight: 390.46
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: {1-methyl-2-[methyl-(toluene-4-sulfonyl)-amino]-2-oxo-ethyl}-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {1-methyl-2-[methyl-(toluene-4-sulfonyl)-amino]-2-oxo-ethyl}-carbamic acid benzyl ester(928342-25-0)
EPA Substance Registry System: {1-methyl-2-[methyl-(toluene-4-sulfonyl)-amino]-2-oxo-ethyl}-carbamic acid benzyl ester(928342-25-0)

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: 928342-25-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 928342-25-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,3,4 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 928342-25:
(8*9)+(7*2)+(6*8)+(5*3)+(4*4)+(3*2)+(2*2)+(1*5)=180
180 % 10 = 0
So 928342-25-0 is a valid CAS Registry Number.

928342-25-0Upstream product

928342-25-0Downstream Products

140668-74-2 2-benzyloxycarbonylamino-thiopropionic acid S-benzyl ester

928342-25-0Relevant academic research and scientific papers

Facile peptide thioester synthesis via solution-phase tosylamide preparation

Manabe, Shino,Sugioka, Tomoyuki,Ito, Yukishige

, p. 849 - 853 (2007/10/03)

Preparation of peptide thioester is essential for native chemical ligation and block condensation. Our novel methodology involves conversion of the carboxylic acid of a peptide into a thioester using p-toluenesulfonyl isocyanate, followed by alkylation, t

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