Cas 214533-91-2,Succinic acid mono-((2R,3R,4S,5R,6S)-4,5-bis-benzyloxy-6-ethylsulfanyl-3-hydroxy-tetrahydro-pyran-2-ylmethyl) ester

214533-91-2

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Basic information

Product Name: Succinic acid mono-((2R,3R,4S,5R,6S)-4,5-bis-benzyloxy-6-ethylsulfanyl-3-hydroxy-tetrahydro-pyran-2-ylmethyl) ester
Synonyms: Succinic acid mono-((2R,3R,4S,5R,6S)-4,5-bis-benzyloxy-6-ethylsulfanyl-3-hydroxy-tetrahydro-pyran-2-ylmethyl) ester
CAS NO:214533-91-2
Molecular Formula:
Molecular Weight: 504.601
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: Succinic acid mono-((2R,3R,4S,5R,6S)-4,5-bis-benzyloxy-6-ethylsulfanyl-3-hydroxy-tetrahydro-pyran-2-ylmethyl) ester(CAS DataBase Reference)
NIST Chemistry Reference: Succinic acid mono-((2R,3R,4S,5R,6S)-4,5-bis-benzyloxy-6-ethylsulfanyl-3-hydroxy-tetrahydro-pyran-2-ylmethyl) ester(214533-91-2)
EPA Substance Registry System: Succinic acid mono-((2R,3R,4S,5R,6S)-4,5-bis-benzyloxy-6-ethylsulfanyl-3-hydroxy-tetrahydro-pyran-2-ylmethyl) ester(214533-91-2)

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: 214533-91-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 214533-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,5,3 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 214533-91:
(8*2)+(7*1)+(6*4)+(5*5)+(4*3)+(3*3)+(2*9)+(1*1)=112
112 % 10 = 2
So 214533-91-2 is a valid CAS Registry Number.

214533-91-2Upstream product

214533-91-2Downstream Products

214533-91-2Relevant academic research and scientific papers

A two-directional approach for the solid-phase synthesis of trisaccharide libraries

Zhu, Tong,Boons, Geert-Jan

, p. 1898 - 1900 (1998)

Without protecting groups, polymer-bound thioglycosyl sugars can undergo two successive glycosylation reactions, once as a donor and once as an acceptor, to give trisaccharides such as 1. Trisaccharide libraries prepared by this strategy have a known suga

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