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3-heptyl-delta(1)-tetrahydrocannabinol, also known as 3HH, is a synthetic cannabinoid that is structurally similar to THC, the main psychoactive component of cannabis. It is a psychoactive compound that acts as a potent and selective agonist of the cannabinoid receptors, particularly the CB1 receptor. 3HH is known for its ability to produce similar effects to THC, such as euphoria, relaxation, and altered perception. However, its pharmacological properties and potential health risks are not yet fully understood, and further research is needed to evaluate its safety and potential medical applications.

54763-99-4

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54763-99-4 Usage

Uses

Used in Pharmaceutical Industry:
3-heptyl-delta(1)-tetrahydrocannabinol is used as a research compound for investigating its potential therapeutic effects. It is being studied for its ability to produce similar effects to THC, which may have potential applications in treating various medical conditions such as pain, anxiety, and spasticity associated with multiple sclerosis.
Used in Drug Development:
3-heptyl-delta(1)-tetrahydrocannabinol is used as a lead compound in the development of new drugs targeting the cannabinoid receptors. Its potent and selective agonist activity at the CB1 receptor makes it a promising candidate for the development of medications with potential therapeutic benefits.
Used in Toxicological Research:
3-heptyl-delta(1)-tetrahydrocannabinol is used as a tool in toxicological research to study the potential health risks and side effects associated with synthetic cannabinoids. Understanding the pharmacological properties and safety profile of 3HH can help in the development of safer and more effective cannabinoid-based therapies.
Note: The uses mentioned above are based on the potential applications of 3-heptyl-delta(1)-tetrahydrocannabinol as a research compound and lead compound in drug development. However, it is important to emphasize that further research is needed to evaluate its safety and potential medical applications before it can be used in any therapeutic or commercial context.

Check Digit Verification of cas no

The CAS Registry Mumber 54763-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,6 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54763-99:
(7*5)+(6*4)+(5*7)+(4*6)+(3*3)+(2*9)+(1*9)=154
154 % 10 = 4
So 54763-99-4 is a valid CAS Registry Number.
InChI:InChI=1/C23H34O2/c1-5-6-7-8-9-10-17-14-20(24)22-18-13-16(2)11-12-19(18)23(3,4)25-21(22)15-17/h13-15,18-19,24H,5-12H2,1-4H3/t18-,19-/m1/s1

54763-99-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (6aR,10aR)-3-heptyl-6,6,9-trimethyl-6a,7,8,10a-tetrahydrobenzo[c]chromen-1-ol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:54763-99-4 SDS

54763-99-4Downstream Products

54763-99-4Relevant academic research and scientific papers

CATALYTIC CANNABINOID PROCESSES AND PRECURSORS

-

, (2020/12/07)

The present disclosure relates to new cannabinoid sulfonate esters and processes for their use to prepare cannabinoids. The disclosure also relates to the use of catalysts and catalytic processes for the preparation of cannabinoids from the cannabinoid sulfonate esters.

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