Cas 682353-86-2,(S)-2-((R)-2-Benzyloxycarbonylamino-4-thiocarboxy-butyrylamino)-propionic acid benzyl ester

682353-86-2

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Basic information

Product Name: (S)-2-((R)-2-Benzyloxycarbonylamino-4-thiocarboxy-butyrylamino)-propionic acid benzyl ester
Synonyms: (S)-2-((R)-2-Benzyloxycarbonylamino-4-thiocarboxy-butyrylamino)-propionic acid benzyl ester
CAS NO:682353-86-2
Molecular Formula:
Molecular Weight: 458.535
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)-2-((R)-2-Benzyloxycarbonylamino-4-thiocarboxy-butyrylamino)-propionic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-((R)-2-Benzyloxycarbonylamino-4-thiocarboxy-butyrylamino)-propionic acid benzyl ester(682353-86-2)
EPA Substance Registry System: (S)-2-((R)-2-Benzyloxycarbonylamino-4-thiocarboxy-butyrylamino)-propionic acid benzyl ester(682353-86-2)

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: 682353-86-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 682353-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,2,3,5 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 682353-86:
(8*6)+(7*8)+(6*2)+(5*3)+(4*5)+(3*3)+(2*8)+(1*6)=182
182 % 10 = 2
So 682353-86-2 is a valid CAS Registry Number.

682353-86-2Upstream product

682353-86-2Downstream Products

682353-86-2Relevant academic research and scientific papers

Synthesis of novel S-neoglycopeptides from glycosylthiomethyl derivatives

Zhu, Xiangming,Pachamuthu, Kandasamy,Schmidt, Richard R.

, p. 1083 - 1085 (2004)

(Equation presented) Reaction of glycosylthiomethyl azides with amino acid and peptide derivatives containing aspartate and glutamate thio acids gave the corresponding glycosylthiomethyl amides in excellent yields. Another type of neoglycopeptides was obt

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