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165524-85-6

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165524-85-6 Usage

General Description

6-O-BENZYL-D-GLUCAL is a chemical compound that belongs to the category of benzyl glycosides. It is a derivative of glucose and contains a benzyl substituent at the 6th position. 6-O-BENZYL-D-GLUCAL, is often used as a building block in organic synthesis and medicinal chemistry. It has been studied for its potential applications in drug development and as a precursor for the synthesis of various bioactive molecules. 6-O-BENZYL-D-GLUCAL has garnered interest due to its unique chemical properties and potential use in the development of new pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 165524-85-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,5,2 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 165524-85:
(8*1)+(7*6)+(6*5)+(5*5)+(4*2)+(3*4)+(2*8)+(1*5)=146
146 % 10 = 6
So 165524-85-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O4/c14-11-6-7-17-12(13(11)15)9-16-8-10-4-2-1-3-5-10/h1-7,11-15H,8-9H2/t11-,12-,13+/m1/s1

165524-85-6SDS

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 (2R,3S,4R)-2-(phenylmethoxymethyl)-3,4-dihydro-2H-pyran-3,4-diol

1.2 Other means of identification

Product number -
Other names 6-benzylglucal

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:165524-85-6 SDS

165524-85-6Downstream Products

165524-85-6Relevant articles and documents

Organoboron-catalyzed regio- and stereoselective formation of β-2-deoxyglycosidic linkages

Beale, Thomas M.,Moon, Patrick J.,Taylor, Mark S.

supporting information, p. 3604 - 3607 (2014/07/21)

A borinic acid derived catalyst enables regioselective and β-selective reactions of 2-deoxy- and 2,6-dideoxyglycosyl chloride donors with pyranoside-derived acceptors having unprotected cis-1,2- and 1,3-diol groups. The use of catalysis to promote a β-sel

Regio- and stereoselectivity of the addition of O-, S-, N-, and C-nucleophiles to the β vinyl oxirane derived from D-glucal

Di Bussolo, Valeria,Caselli, Micaela,Romano, Maria Rosaria,Pineschi, Mauro,Crotti, Paolo

, p. 8702 - 8708 (2007/10/03)

6-O-Trityl- (1a) and 6-(O-benzyl)-substituted epoxide (1b) derived from D-glucal were examined in their addition reactions with O-, C-, N-, and S-nucleophiles. A 1,4-regio- and β-stereoselective or an anti 1,2-addition pathway is commonly observed dependi

Strategy in oligosaccharide synthesis: An application to a concise total synthesis of the KH-1(adenocarcinoma) Antigen

Deshpande, Prashant P.,Kim, Hyunjin M.,Zatorski, Andrzej,Park, Tae-Kyo,Ragupathi, Govindaswami,Livingston, Philip O.,Live, David,Danishefsky, Samuel J.

, p. 1600 - 1614 (2007/10/03)

A concise and potentially practical synthesis of the title compound has been achieved. The route features a high degree of convergence and economy of synthetic operations. A key step is the concurrent introductory addition of three α-1-fucosyl residues at

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