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23050-57-9

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23050-57-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23050-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,5 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23050-57:
(7*2)+(6*3)+(5*0)+(4*5)+(3*0)+(2*5)+(1*7)=69
69 % 10 = 9
So 23050-57-9 is a valid CAS Registry Number.

23050-57-9SDS

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 2-methyl-9-pentyl-5-(propan-2-yl)-3,6-dihydro-2h-2,6-methano-1-benzoxocin-7-ol

1.2 Other means of identification

Product number -
Other names Cannabinol,delta4-isotetrahydro

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:23050-57-9 SDS

23050-57-9Upstream product

23050-57-9Downstream Products

23050-57-9Relevant articles and documents

Isolation, Synthesis And Structure Determination Of Cannabidiol Derivatives And Their Cytotoxic Activities

Nalli, Yedukondalu,Jan, Suraya,Lauro, Gianluigi,Ur Rasool, Javeed,Lone, Waseem I.,Sarkar, Aminur R.,Banday, Junaid,Bifulco, Giuseppe,Laatsch, Hartmut,Syed, Sajad H.,Ali, Asif

, p. 471 - 480 (2019/07/15)

In a continuing effort to explore the structural diversity and pharmacological activities of natural products based scaffolds, herein, we report the isolation, synthesis, and structure determination of cannabidiol and its derivatives along with their cytotoxic activities. Treatment of cannabidiol (1) with acid catalyst POCl3 afforded a new derivative 6 along with six known molecules 2 ? 5, 7 and, 8. The structure of 6 was elucidated by extensive spectroscopic analyses and DFT calculations of the NMR and ECD data. All the compounds (2–8) were evaluated for their cytotoxic potential against a panel of eight cancer cell lines. Compounds 4, 5, 7, and 8 showed pronounced in vitro cytotoxic activity with IC50 values ranging from 5.6 to 60 μM. Out of the active molecules, compounds 4, and 7 were found to be comparable to that of the parent molecule 1 on the inhibition of almost all the tested cancer cell lines.

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