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(±)5-epi CP 55,940

Item No. 13803

Technical Information
Formal Name
rel-5-(1,1-dimethylheptyl)-2-[(1R,2R,5S)-5-hydroxy-2-(3-hydroxypropyl)cyclohexyl]-phenol
CAS Number
2365471-91-4
Molecular Formula
C24H40O3
Formula Weight
Purity
≥97%
Formulation
A solid
DMF: 30 mg/mlDMSO: 30 mg/mlEthanol: 30 mg/mlEthanol:PBS (pH 7.2) (1:3): 0.25 mg/ml
λmax
219, 277 nm
SMILES
O[C@@H]1C[C@@H](C2=CC=C(C(C)(C)CCCCCC)C=C2O)[C@H](CCCO)CC1
InChi Code
InChI=1S/C24H40O3/c1-4-5-6-7-14-24(2,3)19-11-13-21(23(27)16-19)22-17-20(26)12-10-18(22)9-8-15-25/h11,13,16,18,20,22,25-27H,4-10,12,14-15,17H2,1-3H3/t18-,20+,22-/m1/s1
InChi Key
YNZFFALZMRAPHQ-KAGYGMCKSA-N
Regulatory Information
DEA Schedule
I
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    (±)5-epi CP 55,940 (Item No. 13803) is an analytical reference standard that is structurally similar to known synthetic cannabinoids. (±)5-epi CP 55,940 is a potential byproduct in the synthesis of (±)-CP 55,940 (Item No. 13241) based on the published synthesis of (−)-CP 47,497 (Item No. 10917).1,2,3 This product is intended for research and forensic applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Melvin, L.S., Johnson, M.R., Harbert, C.A., et alA cannabinoid derived prototypical analgesic. J. Med. Chem. 27(1), 67-71 (1984).

    2. Johnson, M.R., and Lawrence S.M., J. 2-Hydroxy-4-(substituted) phenyl cycloalkanes and derivatives. (1983).

    3. Hengst, J.A., Nduwumwami, A.J., Raup-Konsavage, W.M., et alInhibition of sphingosine kinase activity enhances immunogenic cell surface exposure of calreticulin induced by the synthetic cannabinoid 5-epi-CP-55,940. Cannabis Cannabinoid Res. 7(5), 637-647 (2022).