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1 References  














4,5-Dihydroorotic acid






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From Wikipedia, the free encyclopedia
 


4,5-Dihydroorotic acid
Names
IUPAC name

2,6-dioxo-1,3-diazinane-4-carboxylic acid

Identifiers

CAS Number

3D model (JSmol)

ChEBI
ChEMBL
ChemSpider
MeSH 4,5-dihydroorotic+acid

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1S/C5H6N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h2H,1H2,(H,9,10)(H2,6,7,8,11) checkY

    Key: UFIVEPVSAGBUSI-UHFFFAOYSA-N checkY

  • InChI=1/C5H6N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h2H,1H2,(H,9,10)(H2,6,7,8,11)

    Key: UFIVEPVSAGBUSI-UHFFFAOYAI

  • O=C1NC(=O)NC(C(=O)O)C1

Properties

Chemical formula

C5H6N2O4
Molar mass 158.112 g/mol

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

☒N verify (what is checkY☒N ?)

Infobox references

4,5-Dihydroorotic acid is a derivative of orotic acid which serves as an intermediate in pyrimidine biosynthesis.[1]

References[edit]

  1. ^ Lacroute F (March 1968). "Regulation of pyrimidine biosynthesis in Saccharomyces cerevisiae". Journal of Bacteriology. 95 (3): 824–832. doi:10.1128/jb.95.3.824-832.1968. PMC 252099. PMID 5651325.


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  • Retrieved from "https://en.wikipedia.org/w/index.php?title=4,5-Dihydroorotic_acid&oldid=1217449116"

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    This page was last edited on 5 April 2024, at 22:04 (UTC).

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