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6(6AR,10AS)-REL-A,7,8,10A-TETRAHYDRO-3,6,6,9-TETRAMETHYL-6H-DIBENZO[B,D]PYRAN-1-OL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

728044-69-7

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728044-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 728044-69-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,8,0,4 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 728044-69:
(8*7)+(7*2)+(6*8)+(5*0)+(4*4)+(3*4)+(2*6)+(1*9)=167
167 % 10 = 7
So 728044-69-7 is a valid CAS Registry Number.

728044-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6(6AR,10AS)-REL-A,7,8,10A-TETRAHYDRO-3,6,6,9-TETRAMETHYL-6H-DIBENZO[B,D]PYRAN-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:728044-69-7 SDS

728044-69-7Downstream Products

728044-69-7Relevant 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.

Biomimetic Cannabinoid Synthesis Revisited: Batch and Flow All-Catalytic Synthesis of (±)-ortho-Tetrahydrocannabinols and Analogues from Natural Feedstocks

Giorgi, Pascal D.,Liautard, Virginie,Pucheault, Mathieu,Antoniotti, Sylvain

, p. 1307 - 1311 (2018/04/02)

Using a combination of Au nanoparticle-catalyzed oxidation under an O2 atmosphere and a Ti-doped montmorillonite (Ti-MMT)-catalyzed tandem arylation/double cyclization, we developed an original and highly selective method for the synthesis of ortho-tetrahydrocannabinol derivatives from simple substrates. The reaction sequence could be performed in two steps in batch mode or in a single operation in continuous-flow reactors. The abnormal regioselectivity was proposed to be the result of the non-innocent role of the MMT support, TiIV cation coordination, and a Lewis acid-assisted Br?nsted acid (LBA) mechanism.

Synthesis of the alkenyl-substituted tetracyclic core of the bisabosquals

Zhou, Jingye,Lobera, Mercedes,Neubert-Langille, Bobbianna J.,Snider, Barry B.

, p. 10018 - 10024 (2008/02/13)

HCl-catalyzed deprotection and cyclization of benzylic alcohol 15 cleanly provided tricycle 16 by a cis-selective intramolecular Diels-Alder reaction. Acetylation of the phenol, bis epoxidation, and base-catalyzed hydrolysis and cyclization afforded tetra

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