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1,2-O-(1-ethoxyethylidene)-6-O-tritylhexopyranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67965-10-0

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67965-10-0 Usage

Chemical structure

A hexopyranose ring with an ethoxyethylidene moiety at the 1,2-position and a trityl group at the 6-position.

Function

Commonly used as a protecting group for the hydroxyl groups on a sugar molecule.

Protection mechanism

The ethoxyethylidene and trityl groups shield the hydroxyl groups from unwanted reactions.

Application

Allows the sugar molecule to undergo specific chemical reactions without interference.

Importance

An important tool in carbohydrate chemistry.

Usage

Utilized for the synthesis of complex sugar-based molecules and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 67965-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,6 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 67965-10:
(7*6)+(6*7)+(5*9)+(4*6)+(3*5)+(2*1)+(1*0)=170
170 % 10 = 0
So 67965-10-0 is a valid CAS Registry Number.

67965-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethoxy-2-methyl-5-(trityloxymethyl)-5,6,7,7a-tetrahydro-3aH-[1,3]dioxolo[4,5-b]pyran-6,7-diol

1.2 Other means of identification

Product number -
Other names 8-ethoxy-8-methyl-3-(trityloxymethyl)-2,7,9-trioxabicyclo[4.3.0]nonane-4,5-diol

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:67965-10-0 SDS

67965-10-0Relevant academic research and scientific papers

Synthesis of the Carbohydrate Moiety of Bleomycin. 1,3,4,6-Tetra-O-substituted L-Gulose Derivatives

Katano, Kiyoaki,Chang, Pei-In,Millar, Alan,Pozsgay, Vince,Minster, David K.,et al.

, p. 5807 - 5815 (2007/10/02)

To facilitate the synthesis of the carbohydrate moiety of bleomycin and its subsequent attachment to the remainder of the bleomycin molecule in a regio- and stereocelective fashion, a number of suita

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