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CP 47497-C6-homolog Preparation Products And Raw materials

CP 47,497-C6 homolog is a synthetic cannabinoid (CB) whose alkyl chain consists of six carbons. While in vitro data suggest that alkylaminoindoles with a side chain length of C4 to C6 possess equal or higher affinity to the CB central CB₁ and peripheral CB₂ receptors compared to Δ⁹–THC, the properties of this compound have not been evaluated. This product is intended for research and forensic applications.

CP 47,497-C6

Uses

CP 47497-C6-homolog is a homolog of CP-47497 (C781310), a cannabinoid receptor ligand. Synthetic cannabinoids

Technical Information

Formal Name

cis–5-(1,1-dimethylhexyl)-2-(3-hydroxycyclohexyl)-phenol

CAS Number

70435-06-2

Molecular Formula

C₂₀H₃₂O₂

Formula Weight

304.5

Purity

≥95%

Formulation(Request formulation change)

A crystalline solid

Solubility

DMF: 10 mg/ml
DMSO: 15 mg/ml
Ethanol: 10 mg/ml
Methanol: 12.5 mg/ml

λ_max

219, 276 nm

SMILES

O[C@H]1C[C@@H](C2=CC=C(C(C)(C)CCCCC)C=C2O)CCC1

InChi Code

InChI=1S/C20H32O2/c1-4-5-6-12-20(2,3)16-10-11-18(19(22)14-16)15-8-7-9-17(21)13-15/h10-11,14-15,17,21-22H,4-9,12-13H2,1-3H3/t15-,17+/m0/s1

InChi Key

KQUGQXNYBWYGAI-DOTOQJQBSA-N

Shipping & Storage Information

Storage

-20°C

Shipping

Room Temperature in continental US; may vary elsewhere

Stability

≥ 2 years

Synthetic cannabinoids
Synthetic cannabinoids are potent agonists of the cannabinoid receptor type 1 (CB1) and type 2 (CB2).

CB1 receptors are distributed in the central and peripheral nervous system, whereas CB2 receptors are distributed outside the nervous system.

Synthetic cannabinoids bind to these cannabinoid receptors stronger than delta9-tetrahydrocannabinol (THC) [9],

the primary psychoactive alkaloid in Cannabis sativa, the plant commonly known as “marijuana” or “hemp,” which has been used as a source of fiber, oil, and medicine and for recreational and religious reasons since antiquity.

Their metabolites also serve as agonists for the CB1 and CB2 receptors. These characteristics account for the stronger potency of synthetic cannabinoids, which make the recreational use of these compounds more dangerous, possibly leading to fatal consequences.

The recreational use of synthetic cannabinoids was first noted in Europe in 2004 and then in the US.

Because of the drastic increase in synthetic cannabinoid-related cases, these compounds were identified as an emerging public health threat in the 2010 annual report of the American Association of Poison Control Centers’ National Poison

Data System (NPDS) in the US. Synthetic cannabinoids were found in herbal incense products known as “K2” or “Spice,” which were sold as legal alternatives to Cannabis-derived products. JWH-018, JWH-073, JWH-250, and JWH-081