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Methyl-1-thio-┈-D-xylopyranoside is a chemical compound with the molecular formula C7H14O4S. It is a derivative of D-xylose, a pentose sugar, where the hydroxyl group at the first carbon has been replaced by a thiomethyl group (-CH3). This modification results in a sulfur-containing sugar analog, which is often used in organic synthesis and as a substrate in enzymatic reactions to study the specificity of glycosidases and other enzymes involved in carbohydrate metabolism. The compound plays a significant role in understanding the interactions between sugars and proteins, as well as in the development of new drugs targeting carbohydrate-active enzymes.

2595-45-1

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2595-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2595-45-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2595-45:
(6*2)+(5*5)+(4*9)+(3*5)+(2*4)+(1*5)=101
101 % 10 = 1
So 2595-45-1 is a valid CAS Registry Number.

2595-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 1-thio-β-D-xylopyranoside

1.2 Other means of identification

Product number -
Other names Methyl-[1-thio-β-D-xylopyranosid]

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 -
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More Details:2595-45-1 SDS

2595-45-1Relevant academic research and scientific papers

Synthesis of O-alpha-D-glucopyranosyl-(1----4)-O-alpha -D-xylopyranosyl-(1----4)-O-alpha -D-xylopyranosyl-(1----4)-D-glucopyranose as a substrate analogue of alpha amylase.

Takeo,Nakagen,Teramoto,Nitta

, p. 261 - 275 (2007/10/02)

The tetrasaccharide a-D-Glcp-(1----4)-a-D-Xylp-(1----4)-a-D-Xylp-(1----4)-D- Glcp (1) has been synthesized, as a substrate analogue of alpha amylase, by silver perchlorate-catalyzed glycosylation of benzyl 2,3,6-tri-O-benzyl-4-O-(2,3-di-O-benzyl-a-D-xylopyranosyl)-beta-D- glucopyranoside (30) with 2,3-di-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-a-D- glucopyranosyl)-a-D-xylopyranosyl chloride or by methyl triflate-promoted condensation of 30 with methyl 2,3-di-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-a-D-glucopyranosyl)-1-thio- beta-D-xylopyranoside, followed by removal of protecting groups of the resulting tetrasaccharide derivative 40.

A Through-process for the Preparation of Methyl Per-O-acetyl 1-Thio-glycosides from Aldoses

Koto, Shinkiti,Yoshida, Toyosaku,Takenaka, Kazuhiro,Zen, Shonosuke

, p. 3667 - 3668 (2007/10/02)

D-Glucose, D-galactose, D-mannose, D-xylose, L-arabinose, L-fucose, L-rhamnose, maltose, cellobiose, lactose, D-glucosamine, D-galactosamine, and D-mannosamine were converted into the corresponding methyl per-O-acetyl 1-thioglycopyranosides by way of a three-step (acetobromination, methylthioation, and acetylation) through-process in a single vessel.

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