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1,3-OXATHIOLANE-2-CARBOXYLIC ACID, 5-HYDROXY- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

672952-08-8

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672952-08-8 Usage

Chemical class

Oxathiolane carboxylic acids

Structural feature

Contains a 5-hydroxy group

Applications

a. Pharmaceutical research and drug development
b. Synthesis of potential drug candidates for various medical conditions
c. Organic chemistry and biochemistry due to its unique structure and reactivity
d. Development of new materials and chemical processes

Reactivity

The 5-hydroxy group may contribute to its reactivity in chemical reactions

Potential uses

May have potential applications in various fields due to its specific chemical properties

Check Digit Verification of cas no

The CAS Registry Mumber 672952-08-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,2,9,5 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 672952-08:
(8*6)+(7*7)+(6*2)+(5*9)+(4*5)+(3*2)+(2*0)+(1*8)=188
188 % 10 = 8
So 672952-08-8 is a valid CAS Registry Number.

672952-08-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-1,3-oxathiolane-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1,3-Oxathiolane-2-carboxylicacid,5-hydroxy

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:672952-08-8 SDS

672952-08-8Relevant academic research and scientific papers

COMPOUNDS FOR USE IN THE TREATMENT OF INFECTIOUS DISEASES

-

Page/Page column 32, (2016/05/02)

The present invention relates to compounds of formula (I), wherein R1, R2, R3, R4, R5 and R6 are as described herein, and their prodrugs or pharmaceutically acceptable salt, enantiomer or diastereomer thereof, and compositions including the compounds and methods of using the compounds.

COMBINED TREATMENT WITH A TLR7 AGONIST AND AN HBV CAPSID ASSEMBLY INHIBITOR

-

Page/Page column 43; 44, (2016/10/04)

The present invention is directed to compositions and methods for treating hepatitis B virus infection. In particular, the present invention is directed to a combination therapy comprising administration of a TLR7 agonist and an HBV capsid assembly inhibi

Practical enantioselective synthesis of lamivudine (3TC) via a dynamic kinetic resolution

Goodyear, Michael D.,Hill, Malcolm L.,West, Jono P.,Whitehead, Andrew J.

, p. 8535 - 8538 (2007/10/03)

A practical enantioselective synthesis of lamivudine 1 is described. A highly effective dynamic kinetic resolution of the 5-hydroxyoxathiolane, followed by chlorination and introduction of cytosine provides an efficient synthesis of lamivudine.

Processes for the diastereoselective separation of nucleoside analogue synthetic intermediates

-

, (2008/06/13)

The present invention relates to highly diastereoselective processes for production of cis-nucleosides and nucleoside analogues and derivatives in high optical purity and intermediates useful in those processes.

Processes for the diastereoselective synthesis of nucleoside analogues

-

, (2008/06/13)

The present invention relates to highly diastereoselective processes for production of cis-nucleosides and nucleoside analogues and derivatives in high optical purity, and intermediates useful in those processes.

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