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14262-83-0

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14262-83-0 Usage

General Description

2,3,4-tri-O-benzoylpentopyranosyl bromide is a chemical compound with the molecular formula C26H21BrO6. It is a derivative of pentopyranosyl bromide and is formed by the substitution of three hydroxyl groups with benzoyl groups. 2,3,4-tri-O-benzoylpentopyranosyl bromide is commonly used in the synthesis of complex carbohydrates and glycoconjugates. Its structure consists of a five-membered ring of carbon atoms, with three benzoyl groups attached to different carbon atoms. It is important in the field of organic chemistry and medicinal research, as it serves as a key intermediate for the introduction of carbohydrates into various biomolecules.

Check Digit Verification of cas no

The CAS Registry Mumber 14262-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,6 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14262-83:
(7*1)+(6*4)+(5*2)+(4*6)+(3*2)+(2*8)+(1*3)=90
90 % 10 = 0
So 14262-83-0 is a valid CAS Registry Number.

14262-83-0SDS

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 (4,5-dibenzoyloxy-6-bromooxan-3-yl) benzoate

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:14262-83-0 SDS

14262-83-0Relevant articles and documents

Convergent strategy for the synthesis of S-linked oligoxylans

Bonora, Beatrice,Boos, Irene,Clausen, Mads H.

, p. 53 - 57 (2017)

Arabinoxylans (AX) are a major class of hemicellulose and an important polysaccharide component of lignocellulosic biomass. To utilize the glycan polymer effectively, it is desirable to learn more about the enzymatic hydrolysis of AXs. Well-defined glycan

Total syntheses of schizandriside, saracoside and (±)-isolariciresinol with antioxidant activities

Sampei, Mana,Arai, Midori A.,Ishibashi, Masami

, p. 651 - 654 (2018/04/16)

Lignans are widely distributed in plants and exhibit significant pharmacological effects, including anti-tumor and antioxidative activities. Here, we describe the total synthesis of schizandriside (1), a compound we previously isolated from Saraca asoca b

Total synthesis of agalloside, isolated from: Aquilaria agallocha, by the 5-O-glycosylation of flavan

Arai, Midori A.,Yamaguchi, Yumi,Ishibashi, Masami

, p. 5025 - 5032 (2017/07/10)

Agalloside (1) is a neural stem cell differentiation activator isolated from Aquilaria agallocha by our group using Hes1 immobilized beads. We conducted the first total synthesis of agalloside (1) via the 5-O-glycosylation of flavan 25 using glycosyl fluoride 20 in the presence of BF3·Et2O. Subsequent oxidation with DDQ to flavanone 2 and deprotection successively provided agalloside (1). This synthetic strategy holds promise for use in the synthesis of 5-O-glycosylated flavonoids. The synthesized agalloside (1) accelerated neural stem cell differentiation, which is a result comparable to that for the naturally occurring compound 1.

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