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Methyl β-D-erythro-3-deoxy-pentofuranoside is a chemical compound with the molecular formula C6H12O4. It is a derivative of pentofuranoside, a type of sugar molecule, where one of the hydroxyl groups has been replaced by a methyl group. methyl β-D-erythro-3-deoxy-pentofuranoside is characterized by its β-D-erythro configuration, which refers to the specific arrangement of atoms in the molecule. It is a synthetic compound that may be used in various chemical and pharmaceutical applications, such as the synthesis of complex carbohydrates or as an intermediate in the production of certain drugs. The compound's structure and properties make it a subject of interest in organic chemistry and biochemistry, particularly in the study of sugar derivatives and their potential biological activities.

4395-36-2

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4395-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4395-36-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,9 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4395-36:
(6*4)+(5*3)+(4*9)+(3*5)+(2*3)+(1*6)=102
102 % 10 = 2
So 4395-36-2 is a valid CAS Registry Number.

4395-36-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl β-D-erythro-3-deoxy-pentofuranoside

1.2 Other means of identification

Product number -
Other names methyl 3-deoxy-β-D-ribofuranoside

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:4395-36-2 SDS

4395-36-2Relevant academic research and scientific papers

Synthesis and Biological Activity of 3'-deoxy Derivatives of Adenosine (5'-N-methylcarboxamide) (MECA)

Volpini, Rosaria,Camaioni, Emidio,Francesco, Emanuela Di,Vittori, Sauro,Fein, Thomas,et al.

, p. S33 - S37 (2007/10/03)

A low affinity adenosine binding protein named adenotin was recently distinguished from adenosine A2A receptors.Its identity or striking amino-terminal homology with stress protein sequences suggests that adenotin could play an important role i

Highly Stereoselective Total Synthesis of 2,5-Anhydro-3-deoxy- and -4-deoxy-D-hexonic Acids and of the Related Deoxyadenosines-C

Gasparini, Fabrizio,Vogel, Pierre

, p. 2451 - 2457 (2007/10/02)

(1R,2S,4R)-2-Cyano-7-oxabicyclohept-5-en-2-yl (1S')-camphanate (5) has been converted into 2,5-anhydro-3-deoxy-D-ribo-hexonic acid (8, eight steps, 38percent) and 2,5-anhydro-3-deoxy-D-xylo-hexonic acid (9, seven steps, 40percent).Similarly, (1S,4S)-7-oxabicyclohept-5-en-3-one ((-)-6, derived from (1S,2R,4S)-2-cyano-7-oxabicyclohept-5-en-2-yl (1R')-camphanate (7) was converted into 2,5-anhydro-4-deoxy-D-ribo-hexonic acid (10, nine steps, 29percent) and 2,5-anhydro-4-deoxy-D-xylo-hexonic acid (11, eight steps, 31percent).The methods exploit the high regioselectivity of the electrophilic additions of the C=C double bonds in 7-oxabicyclohept-5-en-2-yl derivatives 5 and 7 ("naked sugars") and the high exo-face preference for the hydride reduction of 5- and 6-chloro-7-oxabicyclohept-5-en-2-ones (21,35). 2'-Deoxyadenosine-C (12) and cordycepin-C (14) were derived from 8 and 10, respectively.Similarly, the corresponding 2'- and 3'-epimers 13 and 15 (C-nucleosides deriving from 2-deoxy- and 3-deoxy-β-D-threo-pentofuranose, respectively) were obtained in few steps and with high stereoselectivity from 9 and 11, respectively.

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