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Isomer(s)
10849JWH 016
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JWH 073 4-methylnaphthyl analog

Item No. 9001076

Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • 1-butyl-3-(1-(4-methyl)naphthoyl) indole
  • JWH 122 N-butyl analog
Technical Information
Formal Name
(1-butyl-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone
CAS Number
1354631-21-2
Molecular Formula
C24H23NO
Formula Weight
341.5
Purity
≥98%
Formulation
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 15 mg/mlDMSO: 15 mg/mlEthanol: 5 mg/ml
λmax
222, 316 nm
SMILES
O=C(C1=CN(CCCC)C2=C1C=CC=C2)C3=CC=C(C)C4=CC=CC=C43
InChi Code
InChI=1S/C24H23NO/c1-3-4-15-25-16-22(20-11-7-8-12-23(20)25)24(26)21-14-13-17(2)18-9-5-6-10-19(18)21/h5-14,16H,3-4,15H2,1-2H3
InChi Key
DOKBVCMQPGKQGV-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    JWH 073 4-methyl naphthyl analog differs structurally from JWH 073 by having a methyl group added at the 4 position of the naphthyl rings. While the effect of this modification to JWH 073 has not been evaluated, the similar addition to JWH 018 produces JWH 122, which has higher affinities for both central cannabinoid (CB1) (Ki = 9.0 and 0.69, respectively) and peripheral cannabinoid (CB2) receptors (Ki = 2.9 and 1.2, respectively).1 This product is intended for forensic and research purposes only.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Huffman, J.W., Zengin, G., Wu, M.J., et al. Structure-activity relationships for 1-alkyl-3-(1-naphthoyl)indoles at the cannabinoid CB1 and CB2 receptors: Steric and electronic effects of naphthoyl substituents. New highly selective CB2 receptor agonists. Bioorg. Med. Chem. 13(1), 89-112 (2005).