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149966-28-9

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149966-28-9 Usage

Appearance

White to light yellow solid

Molecular weight

239.11 g/mol

Usage

a. Organic synthesis
b. Pharmaceutical research (building block for biologically active molecules)
c. Intermediate in the production of pharmaceuticals and agrochemicals
d. Potential applications in new materials and specialty chemicals development

Safety precautions

a. Handle with care
b. Store in a cool, dry place
c. Keep away from sources of ignition
d. Avoid contact with incompatible materials

Check Digit Verification of cas no

The CAS Registry Mumber 149966-28-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,9,6 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 149966-28:
(8*1)+(7*4)+(6*9)+(5*9)+(4*6)+(3*6)+(2*2)+(1*8)=189
189 % 10 = 9
So 149966-28-9 is a valid CAS Registry Number.

149966-28-9SDS

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 1-(2-bromoethoxymethyl)-4-methoxybenzene

1.2 Other means of identification

Product number -
Other names 1-(2-bromo-ethoxymethyl)-4-methoxy-benzene

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:149966-28-9 SDS

149966-28-9Relevant articles and documents

Development of a Storable Triazinone-Based Reagent for O- p-Methoxybenzylation under Mild Heating Conditions

Fujita, Hikaru,Terasaki, Hiromitsu,Kakuyama, Satoshi,Hioki, Kazuhito,Kunishima, Munetaka

supporting information, (2019/05/08)

A new triazinone-based reagent for O-p-methoxybenzylation has been developed. In spite of its stability in solid form, this reagent converts a free alcohol into the corresponding p-methoxybenzyl ether with mild heating (50-60 °C) in a solution. High funct

6-VINYL PYRIMIDINE AND PYRIMIDINONE DERIVATIVES AND THE USE THEREOF

-

Page/Page column 17, (2010/12/18)

The invention relates to 6-vinyl pyrimidine pyrimidinone derivatives and the use thereof as medicaments in particular for the treatment of HTV infections, the use thereof for preparing pharmaceutical compositions and methods for the preparation thereof.

6-VINYL PYRIMIDINE AND PYRIMIDINONE DERIVATIVES AND THE USE THEREOF

-

Page/Page column 33-34, (2010/11/27)

The invention relates to 6-vinyl pyrimidine pyrimidinone derivatives and the use thereof as medicaments in particular for the treatment of HTV infections, the use thereof for preparing pharmaceutical compositions and methods for the preparation thereof.

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