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94236-21-2

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94236-21-2 Usage

General Description

1-Bromo-2-((Methoxymethoxy)methyl)benzene is a chemical compound with the molecular formula C9H11BrO2. It is a brominated derivative of benzene with a methoxymethoxy group attached to the second carbon atom. 1-broMo-2-((MethoxyMethoxy)Methyl)benzene is commonly used as an intermediate in the synthesis of other organic compounds. It has potential applications in the pharmaceutical and agrochemical industries, as well as in organic synthesis. 1-Bromo-2-((Methoxymethoxy)methyl)benzene is a colorless to pale yellow liquid at room temperature and is typically handled and stored under inert gas to prevent degradation. It is important to handle this compound with caution and use appropriate safety measures due to its potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 94236-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,2,3 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 94236-21:
(7*9)+(6*4)+(5*2)+(4*3)+(3*6)+(2*2)+(1*1)=132
132 % 10 = 2
So 94236-21-2 is a valid CAS Registry Number.

94236-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-2-(methoxymethoxymethyl)benzene

1.2 Other means of identification

Product number -
Other names 2-bromo-1-(methoxymethoxy)methyl 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:94236-21-2 SDS

94236-21-2Relevant articles and documents

Catalytic application of sulfamic acid-functionalized magnetic Fe3O4nanoparticles (SA-MNPs) for protection of aromatic carbonyl compounds and alcohols: Experimental and theoretical studies

Khaef, Sepideh,Taherpour, Avat Arman,Yarie, Meysam,Zolfigol, Mohammad Ali

, p. 44946 - 44957 (2020/12/30)

Protection techniques of functional groups within the structure of organic compounds are important synthetic methods against unwanted attacks from various reagents during synthetic sequences. Acetal and thioacetal groups are well known as protective funct

Copper-catalyzed trifluoromethylation of allylsilanes

Shimizu, Ryo,Egami, Hiromichi,Hamashima, Yoshitaka,Sodeoka, Mikiko

supporting information; experimental part, p. 4577 - 4580 (2012/06/18)

CF3 on Csp3: Trifluoromethylation of allylsilane derivatives was accomplished through the use of CuI and Togni's reagent (1) under mild conditions. The reaction of allylsilanes without a substituent in the 2-position gave vinylsilane derivative

[InCl4]: An efficient catalyst-medium for alkoxymethylation of alcohols and their interconversion to acetates and TMS-ethers

Mohammadpoor-Baltork, Iraj,Moghadam, Majid,Tangestaninejad, Shahram,Mirkhani, Valiollah,Khosropour, Ahmad Reza,Mirjafari, Arsalan

experimental part, p. 568 - 579 (2012/05/05)

A simple, green and chemoselective method for methoxymethylation and ethoxymethylation of primary and secondary alcohols using a Lewis acidic room temperature ionic liquid, [C4mim][InCl4], as catalyst and reaction medium under ambient temperature, microwave and ultrasonic irradiations is reported. In this catalytic system, the corresponding MOM-and EOM-ethers are obtained in excellent yields and in short reaction times. Furthermore, this catalytic system was used for mild and efficient transformations of these protected alcohols to their corresponding acetates and trimethylsilyl ethers under thermal conditions and microwave and ultrasonic irradiations.

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