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185505-15-1

185505-15-1 Structure

185505-15-1 Structure
IdentificationBack Directory
[Name]

(±)-Cannabichromenic Acid
[CAS]

185505-15-1
[Synonyms]

(±)-Cannabichromenic Acid (1.0 mg/mL in Chloroform)
[Molecular Formula]

C22H30O4
[MOL File]

185505-15-1.mol
[Molecular Weight]

358.47
Chemical PropertiesBack Directory
[Boiling point ]

480.8±45.0 °C(Predicted)
[density ]

1.088±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

Acetonitrile: Soluble
Chloroform: Soluble
[pka]

3.25±0.40(Predicted)
[Major Application]

food and beverages
pharmaceutical
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)Exclamation Mark (GHS07)
GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H302+H312+H332-H319
[Precautionary statements ]

P210-P233-P240-P241-P242-P243-P261-P264-P270-P271-P280-P301+P312-P303+P361+P353-P304+P340-P305+P351+P338-P321-P330-P362+P364-P337+P313-P370+P378-P403+P235-P501
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

food and beverages
pharmaceutical
[Definition]

ChEBI: Cannabichromenic acid is a chromenol that is 2H-chromene substituted by methyl, 2-methylpent-2-en-5-yl, hydroxy, carboxy and pentyl groups at positions 2,2,5,6 and 7, respectively. It has a role as an antibacterial agent and a plant metabolite. It is a phytocannabinoid, a hydroxy monocarboxylic acid, a chromenol and an olefinic compound. It is a conjugate acid of a cannabichromenate.
[References]

[1] SATOSHI MORIMOTO. Enzymological Evidence for Cannabichromenic Acid Biosynthesis[J]. Journal of Natural Products , 1997, 60 8: 854-857. DOI: 10.1021/np970210y
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