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58479-67-7

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  • Methyl 2,3,4-tri-O-benzyl-6-O-tert-butyldiphenylsilyl-a-D-glucopyranoside

    Cas No: 58479-67-7

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58479-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58479-67-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,7 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58479-67:
(7*5)+(6*8)+(5*4)+(4*7)+(3*9)+(2*6)+(1*7)=177
177 % 10 = 7
So 58479-67-7 is a valid CAS Registry Number.

58479-67-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2,3,4-tri-O-benzyl-6-O-tert-butyldiphenylsilyl-α-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names METHYL 2,3,4-TRI-O-BENZYL-6-O-TERT-BUTYLDIPHENYLSILYL-A-D-GLUCOPYRANOSIDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58479-67-7 SDS

58479-67-7Relevant articles and documents

Solution- and solid-phase oligosaccharide synthesis using glucosyl iodides: a comparative study

Lam, Son N.,Gervay-Hague, Jacquelyn

, p. 1952 - 1966 (2007/10/03)

Glycosyl iodide donors have been used in both solid- and solution-phase syntheses yielding α-(1->6)-linked glucosyl oligomers in highly efficient protocols. While the solid-phase strategy offers advantages in terms of ease of purification, it requires a t

Novel Silylating Agents Employing 4-Pentenyl Silyl Ethers

Colombier, Caroline,Skrydstrup, Troels,Beau, Jean-Marie

, p. 8167 - 8170 (2007/10/02)

Nonsymmetrical silaketals R'OSiR2OR" other than R = Me were efficiently prepared by the activation of 4-pentenyl silyl ethers with IDCP in the presence of an alcohol.In addition, trialkylsilyl ethers could be prepared from the corresponding trialkylsilyl

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