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728044-69-7

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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

    Cas No: 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

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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 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.

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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