ChemicalBook--->CAS DataBase List--->7699-35-6

7699-35-6

7699-35-6 Structure

7699-35-6 Structure
IdentificationBack Directory
[Name]

(E)-3-(3H-imidazol-4-yl)prop-2-enoic acid
[CAS]

7699-35-6
[Synonyms]

cis-UCA
Nsc407934
cis-Urocanic acid
(Z)-Urocanic acid
Urocanic acid, cis
Cis-Urocanic Acid-[13C3]
(αZ)-1H-Imidazole-4-acrylic acid
(Z)-3-(1H-Imidazole-4-yl)acrylic acid
(2Z)-3-(1H-Imidazole-4-yl)acrylic acid
(Z)-3-(1H-Imidazol-4-yl)propenoic acid
(E)-3-(3H-imidazol-4-yl)prop-2-enoic acid
cis-3-(1H-imidazol-4-yl)-2-propenoic acid
(Z)-3-(3H-imidazol-4-yl)prop-2-enoic acid
2-Propenoic acid, 3-(1H-imidazol-5-yl)-, (2Z)-
cis-3-(1H-imidazol-4-yl)-2-propenoic acid, cis-UCA
[Molecular Formula]

C6H6N2O2
[MDL Number]

MFCD11045310
[MOL File]

7699-35-6.mol
[Molecular Weight]

138.12
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[solubility ]

H2O: >10mg/mL
[form ]

solid (fluffy)
[color ]

white
[Water Solubility ]

Soluble in water
[Sensitive ]

Light Sensitive
Safety DataBack Directory
[Safety Statements ]

22-24/25
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

cis-Urocanic acid is an agonist of the 5-HT2A receptor.
[Definition]

ChEBI: Cis-urocanic acid is a urocanic acid in which the double bond of the carboxyethene moiety has Z configuration. It is a conjugate acid of a cis-urocanate.
[Biochem/physiol Actions]

cis-Urocanic acid (cis-UCA) affects the immune cells of the body and is excreted in the urine due to photoisomerization. It inhibits tumor immunity through photocarcinogenesis in mice. cis-Urocanic acid has been studied to prevent UV-radiation-induced DNA damage leading to skin cancer.
Spectrum DetailBack Directory
[Spectrum Detail]

(E)-3-(3H-imidazol-4-yl)prop-2-enoic acid(7699-35-6)1HNMR
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