Cannabichromene
Structure

- Compound name
- Cannabichromene
- Synonyms
- cannabichrome, pentylcannabichromene or cannabinochromene
- CAS number
- 20675-51-8
- Molecular mass
- 314.469 g/mol
- PubChem
- CBC
CBC is considered one of the “big six” cannabinoids prominent in medical research. For CBC, it converts from CBGA into cannabichrome carboxylic acid (CBCA), and then finally to CBC after exposure to heat or ultraviolet light. CBC is non-intoxicating, so it doesn’t produce a euphoric high like THC. The reason it is non-intoxicating is because it binds poorly to CB1 cannabinoid receptors in the brain. But CBC does bind with other receptors in the body, such as the vanilloid receptor 1 (TRPV1) and transient receptor potential ankyrin 1 (TRPA1), both of which are linked to pain perception. When CBC activates these receptors, increased levels of the body’s natural endocannabinoids like anandamide are released.
