Cas 64534-11-8,methyl 4,6-O-benzylidene-2,3-di-O-(2-hydroxyethyl)-α-D-glucopyranoside

64534-11-8

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Basic information

Product Name: methyl 4,6-O-benzylidene-2,3-di-O-(2-hydroxyethyl)-α-D-glucopyranoside
Synonyms: methyl 4,6-O-benzylidene-2,3-di-O-(2-hydroxyethyl)-α-D-glucopyranoside
CAS NO:64534-11-8
Molecular Formula:
Molecular Weight: 370.4
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: methyl 4,6-O-benzylidene-2,3-di-O-(2-hydroxyethyl)-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 4,6-O-benzylidene-2,3-di-O-(2-hydroxyethyl)-α-D-glucopyranoside(64534-11-8)
EPA Substance Registry System: methyl 4,6-O-benzylidene-2,3-di-O-(2-hydroxyethyl)-α-D-glucopyranoside(64534-11-8)

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: 64534-11-8(Hazardous Substances Data)

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64534-11-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64534-11-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,3 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64534-11:
(7*6)+(6*4)+(5*5)+(4*3)+(3*4)+(2*1)+(1*1)=118
118 % 10 = 8
So 64534-11-8 is a valid CAS Registry Number.

64534-11-8Upstream product

3162-96-7 4,6-O-benzylidene-1-O-methyl-α-D-glucopyranoside

64534-11-8Downstream Products

71088-79-4 methyl 4,6-O-benzylidene-2,3-di-O-(p-toluenesulfonyloxyethyl)-α-D-glucopyranoside

64534-11-8Relevant academic research and scientific papers

Carbohydrate-based aza-macrocycles by Richman-Atkins cyclization of glucopyranose precursors

Rathjens, Andreas,Thiem, Joachim

, p. 18 - 25 (2017)

2, 3-Di-ω-halo- as well as 2, 3-di-ω-toluenesulfonamide-alkylated glucopyranoside derivatives were prepared. Their condensation with α,ω-bis-toluenesulfonamide components under varying Richman-Atkins conditions with alkali carbonate in DMF led to carbohyd

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