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RCS-4 2-methoxy isomer

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    RCS-<wbr/>4 2-<wbr/>methoxy isomer
  • RCS-<wbr/>4 2-<wbr/>methoxy isomer
Cat No: 10865
Biochemicals - Drugs Of Abuse
Cayman

RCS-4 (Item No. 10645) is a synthetic cannabinoid (CB) that has been detected as an adulterant of herbal mixtures.{19508} RCS-4 2-methoxy isomer is an analog of RCS-4 that differs only in the location of the methoxy group on the phenyl ring. The affini...

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Territorial Availability: Available through Bertin Technologies only in France
Technical Warning: Bertin Technologies restricts the sale of this product to licensed controlled substance laboratories and qualified academic research institutions. Please contact us for further details.
Special Advice: Please check regulation status before ordering; additionel fees can apply.
Synonyms:
  • (2-methoxyphenyl)(1-pentyl-1H-indol-3-yl)-methanone
Correlated keywords:
  • synthetic cannabinoids forensics receptors herbal spices incense JWH 250 JWH-250 JWH250 RCS4 RCS 4 analogs CB1 CB2 cannabimimetic indoles CBs analytical references standards
Product Overview:
RCS-4 (Item No. 10645) is a synthetic cannabinoid (CB) that has been detected as an adulterant of herbal mixtures.{19508} RCS-4 2-methoxy isomer is an analog of RCS-4 that differs only in the location of the methoxy group on the phenyl ring. The affinity of RCS-4 2-methoxy isomer for CB receptors, or its physiological effects, have not been documented. However, RCS-4 2-methoxy isomer structurally resembles JWH 250 (Item No. 13634), a cannabimimetic indole that shows a high-affinity for both CB1 and CB2 (Ki = 11 and 33 nM, respectively).{17655}
Size 1 mg
Shipping dry ice
CAS Number 1345966-76-8
Molecular Formula C21H23NO2
SMILES O=C(C1=CC=CC=C1OC)C2=CN(CCCCC)C3=CC=CC=C32
Molecular Weight 321,4
Formulation A solution in methanol
Purity ≥98%
Custom Code 2933.49
UNSPSC code 12352100

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Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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