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2-O,3-O,4-O,5-O-Tetramethyl-D-glucose is a chemical compound derived from D-glucose, a monosaccharide and a primary source of energy for living organisms. In 2-O,3-O,4-O,5-O-Tetramethyl-D-glucose, four hydroxyl groups (-OH) of the D-glucose molecule are replaced by methyl groups (-CH3), resulting in the tetramethylated structure. Specifically, the methyl groups are attached to the 2nd, 3rd, 4th, and 5th carbon atoms of the glucose molecule. This modification alters the chemical and physical properties of the original D-glucose, potentially affecting its solubility, reactivity, and interactions with other molecules. The compound may be used in various applications, such as in the synthesis of complex carbohydrates, as a research tool in biochemistry, or in the development of pharmaceuticals.

4261-26-1

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4261-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4261-26-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,6 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4261-26:
(6*4)+(5*2)+(4*6)+(3*1)+(2*2)+(1*6)=71
71 % 10 = 1
So 4261-26-1 is a valid CAS Registry Number.

4261-26-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name O2,O3,O4,O5-tetramethyl-D-glucose

1.2 Other means of identification

Product number -
Other names 2,3,4,5-tetra-O-methyl-D-glucose

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:4261-26-1 SDS

4261-26-1Downstream Products

4261-26-1Relevant academic research and scientific papers

Asymmetric synthesis using reactions with modest group selectivity

Ward, Dale E.,Liu, YaDong,Rhee, Chung K.

, p. 1429 - 1446 (2007/10/02)

The isomeric purity of products from certain group-selective reactions can be significantly amplified when reactions can occur sequentially.The theoretical basis for a strategy that exploits reactions with modest enantiotopic group selectivity for asymmet

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