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Details

Stereochemistry RACEMIC
Molecular Formula C5H8O3
Molecular Weight 116.1152
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TETRAHYDRO-2-FUROIC ACID

SMILES

OC(=O)C1CCCO1

InChI

InChIKey=UJJLJRQIPMGXEZ-UHFFFAOYSA-N
InChI=1S/C5H8O3/c6-5(7)4-2-1-3-8-4/h4H,1-3H2,(H,6,7)

HIDE SMILES / InChI

Molecular Formula C5H8O3
Molecular Weight 116.1152
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis, structure, magnetic properties and DNA cleavage of binuclear Cu(II) Schiff-base complexes.
2009-04-07
Proline modulates the intracellular redox environment and protects mammalian cells against oxidative stress.
2008-02-15
Intermolecular association of tetrahydrofuran-2-carboxylic acid in solution: a vibrational circular dichroism study.
2006-08-31
Crystal structure of quinohemoprotein alcohol dehydrogenase from Comamonas testosteroni: structural basis for substrate oxidation and electron transfer.
2002-02-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:11:41 GMT 2025
Edited
by admin
on Mon Mar 31 22:11:41 GMT 2025
Record UNII
CJ7M2QK6X3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-521564
Preferred Name English
TETRAHYDRO-2-FUROIC ACID
Systematic Name English
TETRAHYDRO-2-FURANCARBOXYLIC ACID
Systematic Name English
2-FURANCARBOXYLIC ACID, TETRAHYDRO-
Systematic Name English
TERAZOSIN HYDROCHLORIDE IMPURITY, TETRAHYDRO-2-FURANCARBOXYLIC ACID- [USP IMPURITY]
Common Name English
(±)-TETRAHYDRO-2-FUROIC ACID
Systematic Name English
1,2,3,4-TETRAHYDROFURAN-2-CARBOXYLIC ACID
Systematic Name English
(±)-TETRAHYDROFURAN-2-CARBOXYLIC ACID
Systematic Name English
(R,S)-TETRAHYDROFURAN-2-CARBOXYLIC ACID
Systematic Name English
Code System Code Type Description
WIKIPEDIA
Tetrahydro-2-furancarboxylic acid
Created by admin on Mon Mar 31 22:11:41 GMT 2025 , Edited by admin on Mon Mar 31 22:11:41 GMT 2025
PRIMARY
NSC
521564
Created by admin on Mon Mar 31 22:11:41 GMT 2025 , Edited by admin on Mon Mar 31 22:11:41 GMT 2025
PRIMARY
FDA UNII
CJ7M2QK6X3
Created by admin on Mon Mar 31 22:11:41 GMT 2025 , Edited by admin on Mon Mar 31 22:11:41 GMT 2025
PRIMARY
PUBCHEM
86079
Created by admin on Mon Mar 31 22:11:41 GMT 2025 , Edited by admin on Mon Mar 31 22:11:41 GMT 2025
PRIMARY
CAS
16874-33-2
Created by admin on Mon Mar 31 22:11:41 GMT 2025 , Edited by admin on Mon Mar 31 22:11:41 GMT 2025
PRIMARY
EPA CompTox
DTXSID601030927
Created by admin on Mon Mar 31 22:11:41 GMT 2025 , Edited by admin on Mon Mar 31 22:11:41 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
PARENT -> IMPURITY