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19491-18-0

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19491-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19491-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,9 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19491-18:
(7*1)+(6*9)+(5*4)+(4*9)+(3*1)+(2*1)+(1*8)=130
130 % 10 = 0
So 19491-18-0 is a valid CAS Registry Number.

19491-18-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-bromo-3,5-dimethoxybenzoate

1.2 Other means of identification

Product number -
Other names Methyl-2-brom-3,5-dimethoxybenzoat

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:19491-18-0 SDS

19491-18-0Relevant articles and documents

Selective opioid growth factor receptor antagonists based on a stilbene isostere

Stockdale, David P.,Titunick, Michelle B.,Biegler, Jessica M.,Reed, Jessie L.,Hartung, Alyssa M.,Wiemer, David F.,McLaughlin, Patricia J.,Neighbors, Jeffrey D.

, p. 4464 - 4474 (2017)

As part of an ongoing drug development effort aimed at selective opioid receptor ligands based on the pawhuskin natural products we have synthesized a small set of amide isosteres. These amides were centered on lead compounds which are selective antagonis

Regioselective bromination: An approach to the D-ring of the gilvocarcins

Sharif, Ehesan U.,O'Doherty, George A.

, p. 1275 - 1285 (2014)

A method for the regioselective ortho-bromination of unsymmetrically protected 3,5-dihydroxybenzoic acid esters has been developed. The route involves protecting group optimization studies to attain high regioselectivity for the ortho-bromination. Pd-catalyzed stannation and boration were performed to construct the D-ring coupling partners for the synthesis of gilvocarcin analogs.

ENHANCING AUTOPHAGY OR INCREASING LONGEVITY BY ADMINISTRATION OF UROLITHINS OR PRECURSORS THEREOF

-

Sheet 33, (2014/01/17)

Disclosed are methods, compounds, and compositions useful for increasing autophagy and promoting longevity. The methods, compounds, and compositions relate to urolithins and urolithin precursors and use thereof. Certain urolithins are represented by Formula I, while certain urolithin precursors are represented by Formula IV. The urolithin may be urolithin A, urolithin B, urolithin C, or urolithin D. The urolithin precursor may be ellagic acid or an ellagitannin. The methods include in vivo, ex vivo, and in vitro uses of the compounds and compositions.

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