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JWH 073 4-methylnaphthyl analog

Item № 9001076
CAS № 1354631-21-2
Purity ≥98%
product image
                (CAS 1354631-21-2)

Formulation:  A crystalline solid

SIZE PRICE QUANTITY SUBTOTAL
CART TOTAL
     1 mg $65.00 0.00
     5 mg $293.00 0.00
     10 mg $520.00 0.00

Pricing updated 2019-03-26. Prices are subject to change without notice.

Description
Synonyms
  • 1-butyl-3-(1-(4-methyl)naphthoyl) indole
  • JWH 122 N-butyl analog

JWH 073 is a cannabimimetic aminoalkylindole which has been identified in herbal incense.1 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).2 This product is intended for forensic and research purposes only.

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Technical Information
Formal Name
(1-butyl-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone
CAS Number
1354631-21-2
Synonyms
  • 1-butyl-3-(1-(4-methyl)naphthoyl) indole
  • JWH 122 N-butyl analog
Molecular Formula
C24H23NO
Formula Weight
341.5
Purity
≥98%
Formulation
A crystalline solid
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

Warning - this product is not for human or veterinary use.

Shipping & Storage
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Stability
≥ 2 years
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Additional Information

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References & Product Citations
Product Description References

1. Kikura-Hanajiri, R., Uchiyama, N., and Goda, Y. Survey of current trends in the abuse of psychotropic substances and plants in Japan Leg. Med. (Tokyo) 13(3), 109-115 (2011).

2. 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, 89-112 (2005).

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