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89709-04-6

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89709-04-6 Usage

Chemical structure

A glucose molecule with an ethylidene group at the 4 and 6 positions and a phenylmethylcarbonate group attached to the 1 position.

Application in medicinal chemistry

Used for the synthesis of prodrugs, which are inactive forms of a drug that can be converted into the active form in the body.

Stability and bioavailability

The presence of the ethylidene and phenylmethylcarbonate groups can improve the stability and bioavailability of the prodrug.

Value in drug development

Due to its ability to improve stability and bioavailability, this compound is a valuable tool in drug development.

Potential applications

Has potential applications in the field of carbohydrate chemistry.

Building block

Can be used as a building block for the synthesis of more complex carbohydrate derivatives.

Check Digit Verification of cas no

The CAS Registry Mumber 89709-04-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,0 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89709-04:
(7*8)+(6*9)+(5*7)+(4*0)+(3*9)+(2*0)+(1*4)=176
176 % 10 = 6
So 89709-04-6 is a valid CAS Registry Number.

89709-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name β-D-Glucopyranose, 4,6-O-ethylidene-, 1-(phenylmethyl carbonate), (R)-

1.2 Other means of identification

Product number -
Other names 1-0-(Phenylmethylcarbonate)-4,6-O-Ethylidene-Beta-D-Glucopyranoside

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:89709-04-6 SDS

89709-04-6Upstream product

89709-04-6Downstream Products

89709-04-6Relevant articles and documents

A method of preparing intermediates of etoposide (by machine translation)

-

Paragraph 0021; 0044; 0050; 0051, (2018/07/06)

The invention discloses a method of preparing intermediates of etoposide. The method to the 4, 6 - O - acetal - D - glucose as the starting material, in the presence of an acid, with chloromethane acid benzyl ester reaction, to obtain a high yield of 4, 6 - O - acetal - 1 - O - benzyloxycarbonyl - β - D - glucose, then 2, 2 - dichloro acetyl [...] esterification, finally through the catalysis of palladium and reduction to obtain etoposide intermediate 2, 3 - double - O - (2, 2 - II [...]) - 4, 6 - O - ethylidene - β - D - pyran glucose. The material of the invention is cheap, simple and convenient operation, mild reaction conditions, the reaction yield is high, the product has high purity, little pollution to the environment, and is suitable for industrial production. (by machine translation)

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