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2-Furancarboxylic acid, tetrahydro-5-hydroxy-, ethyl ester, (2R)-(9CI) is a chemical compound with the molecular formula C8H12O4. It is a derivative of furancarboxylic acid and belongs to the class of organic compounds known as dialkyl ethers.

208173-52-8

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208173-52-8 Usage

Uses

Used in Pharmaceutical Industry:
2-Furancarboxylic acid, tetrahydro-5-hydroxy-, ethyl ester, (2R)-(9CI) is used as an intermediate in the synthesis of various drugs and as a building block for the preparation of biologically active compounds.
Used in Medicine:
2-Furancarboxylic acid, tetrahydro-5-hydroxy-, ethyl ester, (2R)-(9CI) is used for its therapeutic properties and is being studied for its potential use as an anti-inflammatory and antioxidant agent.
Used in Industrial Applications:
2-Furancarboxylic acid, tetrahydro-5-hydroxy-, ethyl ester, (2R)-(9CI) is used as a solvent and a reagent in chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 208173-52-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,1,7 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 208173-52:
(8*2)+(7*0)+(6*8)+(5*1)+(4*7)+(3*3)+(2*5)+(1*2)=118
118 % 10 = 8
So 208173-52-8 is a valid CAS Registry Number.

208173-52-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-ethyl 5-hydroxytetrahydrofuran-2-carboxylate

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:208173-52-8 SDS

208173-52-8Relevant articles and documents

Anti-HIV and Anti-HBV Activities of L-2',3'-dideoxynucleoside Analogues: ddC, 5FddC, 5-Aza ddC and ddG

Mansour, Tarek S.,Tse, Allan,Charron, Marie,Hooker, Elizabeth U.,Ashman, Clare,et al.

, p. 417 - 425 (2007/10/03)

The antiviral activities of the L-enantiomers of the title nucleoside analogues were determined in vitro. β-L-ddC and β-L-5FddC showed significant activity against the replication of HIV-1 and HBV, whereas β-L-5-aza ddC and β-L-ddG were devoid of such activities.

Diastereocontrol in Glycosylation Reactions: Synthesis of β-D and β-L Dideocytidine Analogues

Tse, Allan,Mansour, Tarek S.

, p. 7807 - 7810 (2007/10/02)

Expeditious and diastereoselective total syntheses of the antiviral agents, β-L-ddC, β-L-5FddC and β-D-5FddC have been achieved in four steps from commercially available R-(-)-5-oxo-2-tetrahydrofurancarboxylic and its 2S isomer respectively.

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