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1972-05-0

Cannabidiol-3-monomethyl ether (CBDMME) is a synthetic, non-psychoactive cannabinoid analog derived from cannabidiol (CBD), a naturally occurring compound found in the cannabis plant. It is structurally similar to CBD but with a methyl group attached to the oxygen atom in the ether linkage, which differentiates it from its parent compound. CBDMME has been studied for its potential therapeutic effects, particularly in the areas of pain management, inflammation, and neuroprotection. However, it is important to note that research on CBDMME is still in its early stages, and its safety and efficacy have not been fully established. As with any substance, it is crucial to consider the legal status and potential risks associated with its use, as regulations and scientific understanding continue to evolve.

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  • 1972-05-0 Structure

  • Basic information

    1. Product Name: cannabidiol-3-monomethyl ether
    2. Synonyms: cannabidiol-3-monomethyl ether
    3. CAS NO:1972-05-0
    4. Molecular Formula: C22H32O2
    5. Molecular Weight: 328.48828
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1972-05-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 418°Cat760mmHg
    3. Flash Point: 142.1°C
    4. Appearance: /
    5. Density: 0.988g/cm3
    6. Vapor Pressure: 1.4E-07mmHg at 25°C
    7. Refractive Index: 1.524
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: cannabidiol-3-monomethyl ether(CAS DataBase Reference)
    11. NIST Chemistry Reference: cannabidiol-3-monomethyl ether(1972-05-0)
    12. EPA Substance Registry System: cannabidiol-3-monomethyl ether(1972-05-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1972-05-0(Hazardous Substances Data)

1972-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1972-05-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,7 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1972-05:
(6*1)+(5*9)+(4*7)+(3*2)+(2*0)+(1*5)=90
90 % 10 = 0
So 1972-05-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H32O2/c1-6-7-8-9-17-13-20(23)22(21(14-17)24-5)19-12-16(4)10-11-18(19)15(2)3/h12-14,18-19,23H,2,6-11H2,1,3-5H3/t18-,19+/m0/s1

1972-05-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Cannabidiol monomethyl ether

1.2 Other means of identification

Product number -
Other names CBDM

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:1972-05-0 SDS

1972-05-0Relevant articles and documents

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.

O-Methyl Phytocannabinoids: Semi-synthesis, Analysis in Cannabis Flowerheads, and Biological Activity

Caprioglio, Diego,Allegrone, Gianna,Pollastro, Federica,Valera, Stefano,Lopatriello, Annalisa,Collado, Juan A.,Munoz, Eduardo,Appendino, Giovanni,Taglialatela-Scafati, Orazio

, p. 981 - 986 (2019/08/20)

A general protocol for the selective mono-O-methylation of resorcinyl phytocannabinoids was developed. The availability of semisynthetic monomethyl analogues of cannabigerol, cannabidiol, and cannabidivarin (1a-3a, respectively) made it possible to quanti

Enantioselective Total Synthesis of Cannabinoids - A Route for Analogue Development

Shultz, Zachary P.,Lawrence, Grant A.,Jacobson, Jeffrey M.,Cruz, Emmanuel J.,Leahy, James W.

, p. 381 - 384 (2018/01/27)

A practical synthetic approach to Δ9-tetrahydrocannabinol (1) and cannabidiol (2) that provides scalable access to these natural products and should enable the generation of novel synthetic analogues is reported.

A One-Step Method for the α-Arylation of Camphor. Synthesis of (-)-Cannabidiol and (-)-Cannabidiol Dimethyl Ether

Vaillancourt, Valerie,Albizati, Kim F.

, p. 3627 - 3631 (2007/10/02)

The syntheses of (-)-cannabidiol and (-)-cannabidiol dimethyl ether were accomplished via fragmentation of an appropriately substituted 9-bromocamphor derivative.A new method of α-arylation of 3,9-dibromocamphor was shown to provide a variety of α-arylated camphor derivatives in good yields.

BORON TRIFLUORIDE ETHERATE ON ALUMINA - A MODIFIED LEWIS ACID REAGENT. AN IMPROVED SYNTHESIS OF CANNABIDIOL.

Baek, Seung-Hwa,Srebnik, Morris,Mechoulam, Raphael

, p. 1083 - 1086 (2007/10/02)

Boron trifluoride etherate on alumina catalyses the condensation of resorcinols and monomethyl resorcinols with several monoterpenoid allylic alcohols: in contrast to paralell reactions with boron trifluoride etherate in solution the products obtained do not undergo further cyclisations.

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