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Methyl α-D-galactofuranoside is a naturally occurring sugar derivative, specifically a methyl glycoside of α-D-galactofuranose. It is a monosaccharide, which is a simple form of sugar, and is part of a class of compounds known as furanoses. This chemical is significant in the field of carbohydrate chemistry and is often used in research to study the structure and function of complex carbohydrates. It plays a role in various biological processes, including cell recognition and communication, and can be found in certain types of plant cell walls and microbial polysaccharides. The compound is also of interest in the development of new drugs and vaccines due to its potential interactions with biological systems.

3795-67-3

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3795-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3795-67-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,9 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3795-67:
(6*3)+(5*7)+(4*9)+(3*5)+(2*6)+(1*7)=123
123 % 10 = 3
So 3795-67-3 is a valid CAS Registry Number.

3795-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl α-D-galactofuranoside

1.2 Other means of identification

Product number -
Other names Methyl-α-D-galaktofuranosid

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:3795-67-3 SDS

3795-67-3Downstream Products

3795-67-3Relevant academic research and scientific papers

Methyl glycosides via Fischer glycosylation: translation from batch microwave to continuous flow processing

Aronow, Jonas,Stanetty, Christian,Baxendale, Ian R.,Mihovilovic, Marko D.

, p. 11 - 19 (2018/11/27)

Abstract: A continuous flow procedure for the synthesis of methyl glycosides (Fischer glycosylation) of various monosaccharides using a heterogenous catalyst has been developed. In-depth analysis of the isomeric composition was undertaken and high consistency with corresponding results observed under microwave heating was obtained. Even in cases where addition of water was needed to achieve homogeneity—a prerequisite for the flow experiments—no detrimental effect on the conversion was found. The scalability was demonstrated on a model case (mannose) and as part of the target-oriented synthesis of d-glycero-d-manno heptose, both performed on multigram scale.

Kinetic products under thermal conditions: Rapid entry into α/β-D-galactofuranosides using microwave irradiation and selective Lewis acids

Santra, Soumava,Jonas, Emily,Bourgault, Jean-Paul,El-Baba, Tarick,Andreana, Peter R.

experimental part, p. 27 - 40 (2012/01/17)

A modified Fischer-Lubineau reaction, employing microwave irradiation and selected Lewis acids such as Mn(ClO4)2, Mn(C 2H3O2)3, FeCl3, CoCl 2, and AgF as independent a

Facile synthesis of methyl α- and β-d-[6-3H]galactofuranosides from d-galacturonic acid. Substrates for the detection of galactofuranosidases

Bordoni, Andrea,Lima, Carlos,Marino, Karina,de Lederkremer, Rosa M.,Marino, Carla

, p. 1863 - 1869 (2008/12/22)

Galactofuranose metabolism is a good target for the development of novel chemotherapeutic agents for the treatment of some microbial infections. A simple procedure for the synthesis of methyl (methyl α,β-d-galactopyranosid)uronate followed by NaB3H4 reduction gave a straightforward access to radiolabeled substrates for galactofuranosidases.

High-yielding one-step conversion of D-glucose and D-galactose to the corresponding α and β methyl-D-glucofuranosides and galactofuranosides

Lubineau,Fischer

, p. 815 - 818 (2007/10/02)

D-Glucose and D-Galactose are transformed to the corresponding α and β-Methyl D-Glucofuranosides in good yields using methanol and Ferric chloride as catalyst.

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