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55824-11-8

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55824-11-8 Usage

Description

Cannabigerovarol (CBGV) is a minor cannabinoid found in cannabis plants, structurally related to other cannabinoids such as cannabigerol (CBG) and cannabidiol (CBD). It is a non-psychoactive compound with potential therapeutic benefits, including anti-inflammatory, neuroprotective, and anti-cancer properties. Further research is needed to fully understand its pharmacological properties and potential medical applications.

Uses

Used in Pharmaceutical Industry:
Cannabigerovarol is used as a therapeutic agent for its potential anti-inflammatory, neuroprotective, and anti-cancer properties. It may help in managing inflammation, protecting the nervous system, and fighting cancer cells.
Used in Cosmetic Industry:
Cannabigerovarol is used as an ingredient in cosmetic products for its potential anti-inflammatory and skin-soothing properties, making it suitable for skincare formulations.
Used in Nutraceutical Industry:
Cannabigerovarol is used as a supplement in the nutraceutical industry for its potential health benefits, including its anti-inflammatory and neuroprotective properties.
Used in Drug Development:
Cannabigerovarol is used in drug development for its potential therapeutic benefits, with ongoing research to explore its pharmacological properties and medical applications further.

Check Digit Verification of cas no

The CAS Registry Mumber 55824-11-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,2 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55824-11:
(7*5)+(6*5)+(5*8)+(4*2)+(3*4)+(2*1)+(1*1)=128
128 % 10 = 8
So 55824-11-8 is a valid CAS Registry Number.

55824-11-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-propyl-benzene-1,3-diol

1.2 Other means of identification

Product number -
Other names Cannabigerovarin

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:55824-11-8 SDS

55824-11-8Relevant articles and documents

CATALYTIC CANNABIGEROL PROCESSES AND PRECURSORS

-

, (2021/10/11)

The present disclosure relates to cannabigerol sulfonate esters and processes for their use to prepare cannabigerol (CBG) and related compounds, including cannabigerobutol (CBGB), cannabigerovarin (CBGV), and cannabigerophorbol (CBGP). In a preferred embodiment, the cannabigerol sulfonate ester is (E)-4-(3, 7-5 dimethylocta-2,6-dienyl)-3,5-bis(trimetbylsilyloxy)phenyl trifluoromethanesulfonate. In a preferred process, the trifluoromethansulfonate leaving group is replaced by an alkyl group. The disclosure also relates to the use of catalysts and catalytic processes for the preparation of cannabigerol and related compounds from the cannabigerol sulfonate esters.

APPARATUS AND METHODS FOR THE SIMULTANEOUS PRODUCTION OF CANNABINOID COMPOUNDS

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Page/Page column 71, (2016/03/22)

The present invention provides an apparatus and methods for simultaneously producing different compounds in various ratios under set conditions.

Cannabis. X. The isolation and structures of four new propyl cannabinoid acids, tetrahydrocannabivarinic acid, cannabidivarinic acid, cannabichromevarinic acid and cannabigerovarinic acid, from Thai cannabis, Meao Variant

Shoyama,Hirano,Makino,et al.

, p. 2306 - 2311 (2007/10/11)

Four new cannabinoids acids, tetrahydrocannabivarinic acid, cannabidivarinic acid, cannabichromevarinic acid and cannabigerovarinic acid were isolated from Thai Cannabis 'Meao variant' and these structures were elucidated on the basis of chemical and spectral data. This is the first example of the isolation of propyl cannabinoid acid from Cannabis.

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