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13241-00-4

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13241-00-4 Usage

Chemical Properties

White Solid

Uses

This compound has been shown to stimulate gustatory receptors, specifically those responsible for sweet taste in mammalian biochemical studies. It is also an intermediate for the synthesis of 4-Deoxy-D-glucose.

Check Digit Verification of cas no

The CAS Registry Mumber 13241-00-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,4 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13241-00:
(7*1)+(6*3)+(5*2)+(4*4)+(3*1)+(2*0)+(1*0)=54
54 % 10 = 4
So 13241-00-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O5/c1-11-7-6(10)5(9)2-4(3-8)12-7/h4-10H,2-3H2,1H3/t4?,5-,6-,7-/m0/s1

13241-00-4SDS

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 4-deoxy-α-D-galactopyranoside

1.2 Other means of identification

Product number -
Other names -

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:13241-00-4 SDS

13241-00-4Relevant articles and documents

Synthesis of Deoxyglycosides by Desulfurization under UV Light

Ge, Jian-Tao,Li, Ying-Ying,Tian, Jun,Liao, Rong-Zhen,Dong, Hai

, p. 7008 - 7014 (2017/07/15)

This study was performed to develop a highly efficient method whereby desulfurization could be completed in 0.5 h under ultraviolet light, at room temperature, and in the presence of trialkylphosphine. Using this method, deoxyglycosides could be produced from sulfur-containing glycosides in almost quantitative yields. The much higher reactivity of desulfurization with triethylphosphine versus that with triethylphosphite is also discussed.

TOTAL ASYMMETRIC SYNTHESES OF 3- AND 4-DEOXY-HEXOSES AND DERIVATIVES.

Fattori, Daniela,Vogel, Pierre

, p. 10587 - 10602 (2007/10/02)

(1S,4S)-7-Oxabicyclohept-5-en-2-one ((-)-5, a "naked sugar") has been converted to (-)-(1R,4S,6S)-6-endo-benzyloxy-2-bromo-7-oxabicyclohept-2-ene ((-)-12) in a highly stereoselective fashion.Double hydroxylation of the C=C double bond of (-)

SYNTHESIS OF SOME DEOXY, UNSATURATED, AND DIDEOXY SUGARS VIA REGIOSELECTIVE THIOACYLATION OF GLYCOPYRANOSIDES BY THE DIBUTYLTIN OXIDE METHOD

Haque, Md. Ekramul,Kikuchi, Tohoru,Kanemitsu, Kimihiro,Tsuda, Yoshisuke

, p. 430 - 433 (2007/10/02)

Treatment of non-protected glycopyranosides (Me α-D-Glc, Me β-D-Glc, Me α-D-Xyl, and Me β-D-Xyl) with dibutyltin oxide followed by thioacylation with phenoxythiocarbonyl chloride gave the mono-thionocarbonates regioselectively in high yields.Acetylation o

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