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14045-42-2

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14045-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14045-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,4 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14045-42:
(7*1)+(6*4)+(5*0)+(4*4)+(3*5)+(2*4)+(1*2)=72
72 % 10 = 2
So 14045-42-2 is a valid CAS Registry Number.

14045-42-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dibromo-5-(methoxymethyl)benzene-1,2-diol

1.2 Other means of identification

Product number -
Other names lanosol methyl ether

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:14045-42-2 SDS

14045-42-2Downstream Products

14045-42-2Relevant articles and documents

-

Weinstein,B. et al.

, p. 2667 - 2670 (1975)

-

In-vitro cytotoxic activities of the major bromophenols of the red alga Polysiphonia lanosa and some novel synthetic isomers

Shoeib, Nagwa A.,Bibby, Michael C.,Blunden, Gerald,Linley, Peter A.,Swaine, David J.,Wheelhouse, Richard T.,Wright, Colin W.

, p. 1445 - 1449 (2007/10/03)

Bioassay-guided fractionation was applied to the cytotoxic chloroform fraction of the red alga Polysiphonia lanosa. The major compounds of the most active fraction were identified using GLC-MS analysis as lanosol (1), methyl, ethyl, and n-propyl ethers of lanosol (1a, 1b, and 1c, respectively), and aldehyde of lanosol (2), although 1b appears to be an artifact arising during the fractionation procedure. These compounds and other known bromophenols were synthesized in addition to four novel isomers (3, 3a-c). The cytotoxic activities of all the synthetic compounds were determined against DLD-1 cells using the MTT assay. Compounds with IC50 50 = 1.72 and 0.80 μmol, respectively), and its effect on the cell cycle was studied using flow cytometry.

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