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10343-13-2

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  • BENZYL 2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSIDE

    Cas No: 10343-13-2

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10343-13-2 Usage

Chemical Properties

White Solid

Check Digit Verification of cas no

The CAS Registry Mumber 10343-13-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,4 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10343-13:
(7*1)+(6*0)+(5*3)+(4*4)+(3*3)+(2*1)+(1*3)=52
52 % 10 = 2
So 10343-13-2 is a valid CAS Registry Number.

10343-13-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzyl 2,3,4,6-Tetra-O-acetyl-?-D-Glucopyranoside

1.2 Other means of identification

Product number -
Other names [(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-phenylmethoxyoxan-2-yl]methyl acetate

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:10343-13-2 SDS

10343-13-2Relevant articles and documents

Amberlyst 15 as a mild and effective activator for the glycosylation with disarmed glycosyl trichloroacetimidate donors

Tian, Qiang,Zhang, Shuo,Yu, Qian,He, Mei-Bo,Yang, Jin-Song

, p. 2142 - 2147 (2007)

Amberlyst 15 acidic resin has been shown to be a mild and effective activator for the glycosylation with commonly used disarmed glycosyl trichloroacetimidate donors. Glucosylation, galactosylation, rhamnosylation, and lactosylation of a panel of representative alcohol and thiol acceptors promoted by Amberlyst 15 allowed for the formation of structurally diverse O- or S-linked oligosaccharides and glycosylated amino acids in moderate to excellent yields.

Synthesis of glycosides via indium(III) chloride mediated activation of glycosyl halide in neutral condition

Mukherjee, Debaraj,Kumar Ray, Pradip,Sankar Chowdhury, Uday

, p. 7701 - 7704 (2001)

Various glycosides and disaccharides were synthesized through coupling of glycosyl bromides with acceptors in presence of indium chloride as a promoter. Glycosidation reactions proceeded with high stereoselectivity.

PHENOLIC PLANT GROWTH INHIBITORS FROM THE FLOWERS OF CUCURBITA PEPO

Itokawa, Hideji,Oshida, Yoshiaki,Ikuta, Akira,Inatomi, Hideo,Adachi, Takashi

, p. 1935 - 1938 (1982)

Eleven compounds isolated from the growth inhibiting active fraction of male flowers of Cucurbita pepo, were identified as p-hydroxybenzaldehyde, anisyl alcohol, p-hydroxybenzyl methyl ether, p-hydroxybenzyl alcohol, veratryl alcohol, isovanillyl alcohol, p-coumaric acid, phloretic acid, benzyl-β-D-glucoside, 4-methoxybenzyl-β-D-glucoside ans 3,4-dimethoxybenzyl-β-D-glucoside.Each compound was assayed for growth inhibiting activity using lettuce seedlings; three showed strong activity, whereas the glucosides were inactive.Key Word Index - Cucurbita pepo; Cucurbitaceae; male flowers; plant growth inhibitor; benzyl glucoside; 4-methoxybenzyl glucoside; 3,4-methoxybenzyl glucoside.

Bemiller,Muenchov

, p. 253,254-262 (1973)

Organocatalysis Linked to Charge-Enhanced Acidity with Superelectrophilic Traits

Smajlagic, Ivor,White, Brandon,Azeez, Oyindamola,Pilkington, Melanie,Dudding, Travis

, p. 1128 - 1138 (2022/01/19)

Hydrogen bonding is ubiquitous throughout nature and serves as a versatile platform for accessing chemical reactivity. In leveraging this force, chemists have utilized organocatalysts to expand the spectrum of chemical reactivity enabled by hydrogen bondi

INHIBITORS OF MALARIAL AND PLASMODIUM FALCIPARUM HEXOSE TRANSPORTER AND USES THEREOF

-

Paragraph 00513, (2021/08/14)

Provided are molecules capable of binding to binding pockets of Plasmodium falciparum hexose transporter (PfHT) or analogs thereof and complexes comprising the same. Also provided herein are inhibitors of PfHT, pharmaceutical compositions comprising the i

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