Cas 405236-13-7,4-Methyl-benzoic acid (2S,3R,4S,5S,6R)-5-benzyloxy-6-benzyloxymethyl-4-(2-chloro-acetoxy)-2-phenylsulfanyl-tetrahydro-pyran-3-yl ester

405236-13-7

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Basic information

Product Name: 4-Methyl-benzoic acid (2S,3R,4S,5S,6R)-5-benzyloxy-6-benzyloxymethyl-4-(2-chloro-acetoxy)-2-phenylsulfanyl-tetrahydro-pyran-3-yl ester
Synonyms: 4-Methyl-benzoic acid (2S,3R,4S,5S,6R)-5-benzyloxy-6-benzyloxymethyl-4-(2-chloro-acetoxy)-2-phenylsulfanyl-tetrahydro-pyran-3-yl ester
CAS NO:405236-13-7
Molecular Formula:
Molecular Weight: 647.189
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: 4-Methyl-benzoic acid (2S,3R,4S,5S,6R)-5-benzyloxy-6-benzyloxymethyl-4-(2-chloro-acetoxy)-2-phenylsulfanyl-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-Methyl-benzoic acid (2S,3R,4S,5S,6R)-5-benzyloxy-6-benzyloxymethyl-4-(2-chloro-acetoxy)-2-phenylsulfanyl-tetrahydro-pyran-3-yl ester(405236-13-7)
EPA Substance Registry System: 4-Methyl-benzoic acid (2S,3R,4S,5S,6R)-5-benzyloxy-6-benzyloxymethyl-4-(2-chloro-acetoxy)-2-phenylsulfanyl-tetrahydro-pyran-3-yl ester(405236-13-7)

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: 405236-13-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 405236-13-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,5,2,3 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 405236-13:
(8*4)+(7*0)+(6*5)+(5*2)+(4*3)+(3*6)+(2*1)+(1*3)=107
107 % 10 = 7
So 405236-13-7 is a valid CAS Registry Number.

405236-13-7Upstream product

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405236-13-7Relevant academic research and scientific papers

Solid-phase capture-release strategy applied to oligosaccharide synthesis on a soluble polymer support

Ando, Hiromune,Manabe, Shino,Nakahara, Yoshiaki,Ito, Yukishige

, p. 4725 - 4728 (2007/10/03)

A highly simplified synthesis of a tetrasaccharide was possible by a repeated coupling/capture-release cycle. In the first cycle, a glycosyl acceptor (1) bound to a soluble polymer reacted with a glycosyl donor (2) having a chloroacetyl group as a tempora

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