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1'-Naphthoyl-2-methylindole

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    1'-<wbr/>Naphthoyl-<wbr/>2-<wbr/>methylindole
  • 1'-<wbr/>Naphthoyl-<wbr/>2-<wbr/>methylindole
Cat No: 14801
Biochemicals - Analytical Standards
Cayman

A large number of synthetic cannabinoids (CBs) have been detected in herbal blends sold for recreational use.{19508} 1’-Naphthoyl indole represents the simplest form of this group of cannabimimetics. While the addition of an N-alkyl chain of four or mo...

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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-methyl-1H-indol-3-yl)-1-naphthalenyl-methanone
Correlated keywords:
  • CBs cannabinoids forensics sciences cannabimimetics CB1 CB2 receptors agonists spices synthetic analytical references standards herbal blends N-alkyl alkyl chains carbons central peripheral naphthoyls methylindoles recreational use 1’-naphthoyl indoles 1s 1’ additions 4s activates shorts inactives affinity 1’-naphthoyl-2-methylindole 2s methyls groups positions rings research applications
Product Overview:
A large number of synthetic cannabinoids (CBs) have been detected in herbal blends sold for recreational use.{19508} 1’-Naphthoyl indole represents the simplest form of this group of cannabimimetics. While the addition of an N-alkyl chain of four or more carbons generates compounds which potently activate CB receptors, short chain lengths are inactive at both central CB1 and peripheral CB2.{16797} This suggests that 1’-naphthoyl indole should have no appreciable affinity for either receptor. 1’-Naphthoyl-2-methylindole differs structurally from 1’-naphthoyl indole by having a methyl group attached at the two position of the indole ring. The biological activities of this compound have not been characterized. This product is intended for forensic and research applications.
Size 5 mg
Shipping dry ice
CAS Number 80749-33-3
Molecular Formula C20H15NO
SMILES O=C(C1=C(C)NC2=C1C=CC=C2)C3=CC=CC4=C3C=CC=C4
Molecular Weight 285,4
Formulation A crystalline solid
Purity ≥98%
Custom Code 3822.19
UNSPSC code 12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

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.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.

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