Cas 130632-55-2,2,3,4,6-tetra-O-benzyl-1-C-methyl-α-D-glucopyranosyl dimethylphosphinothioate

130632-55-2

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Basic information

Product Name: 2,3,4,6-tetra-O-benzyl-1-C-methyl-α-D-glucopyranosyl dimethylphosphinothioate
Synonyms: 2,3,4,6-tetra-O-benzyl-1-C-methyl-α-D-glucopyranosyl dimethylphosphinothioate
CAS NO:130632-55-2
Molecular Formula:
Molecular Weight: 646.785
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: 2,3,4,6-tetra-O-benzyl-1-C-methyl-α-D-glucopyranosyl dimethylphosphinothioate(CAS DataBase Reference)
NIST Chemistry Reference: 2,3,4,6-tetra-O-benzyl-1-C-methyl-α-D-glucopyranosyl dimethylphosphinothioate(130632-55-2)
EPA Substance Registry System: 2,3,4,6-tetra-O-benzyl-1-C-methyl-α-D-glucopyranosyl dimethylphosphinothioate(130632-55-2)

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: 130632-55-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 130632-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,3 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 130632-55:
(8*1)+(7*3)+(6*0)+(5*6)+(4*3)+(3*2)+(2*5)+(1*5)=92
92 % 10 = 2
So 130632-55-2 is a valid CAS Registry Number.

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130632-55-2Relevant academic research and scientific papers

Synthesis of 1-C-alkyl-α-d-glucopyranosides by Lewis acid- or Br?nsted acid-catalyzed O-glycosidation

Yamanoi, Takashi,Oda, Yoshiki,Matsuda, Sho,Yamazaki, Ippo,Matsumura, Kazuhide,Katsuraya, Kaname,Watanabe, Mikio,Inazu, Toshiyuki

, p. 10383 - 10392 (2007/10/03)

We prepared several kinds of 1-C-alkyl-2,3,4,6-tetra-O-benzyl-α-d-glucopyranose derivatives containing methyl, ethyl, n-butyl, and benzyl groups as the alkyl groups at their anomeric positions. The Lewis acid- or Br?nsted acid-catalyzed O-glycosidations u

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