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3771-13-9

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3771-13-9 Usage

General Description

2-(Bromomethyl)-1-chloro-4-methoxybenzene is a complex organic compound falling under the category of aromatic halides. As such, it features a benzene ring as its core structural component, and is characterized by the presence of bromomethyl (a bromine atom bounded to a methyl group), chloro (indicating a chlorine atom), and methoxy (a methyl group linked to an oxygen atom) functional groups. Its chemical characteristics, reactivity, and potential uses generally depend on these functional groups. Given its detailed structure, this chemical compound is likely used in specialized fields such as synthetic organic chemistry or pharmaceutical research. However, detailed information about its specific applications, safety, and toxicity considerations is not commonly available and would likely require specialist knowledge or resources to fully understand.

Check Digit Verification of cas no

The CAS Registry Mumber 3771-13-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,7 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3771-13:
(6*3)+(5*7)+(4*7)+(3*1)+(2*1)+(1*3)=89
89 % 10 = 9
So 3771-13-9 is a valid CAS Registry Number.

3771-13-9SDS

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-(Bromomethyl)-1-chloro-4-methoxybenzene

1.2 Other means of identification

Product number -
Other names 2-chloro-5-methoxy-benzyl bromide

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:3771-13-9 SDS

3771-13-9Relevant articles and documents

Synthesis of polycyclic molecules by double C(sp2)-H/C(sp 3)-H arylations with a single palladium catalyst

Pierre, Cathleen,Baudoin, Olivier

supporting information; experimental part, p. 1816 - 1819 (2011/06/21)

Polycyclic molecules were obtained in good yields by double C(sp 2)-H/C(sp3)-H arylations mediated by a single palladium/phosphine catalyst. Both double intermolecular/intramolecular and intramolecular/intramolecular C-C couplings we

1-(2,6-Dichloro-4-hydroxyphenyl)-2-phenylethanes - New biological response modifiers for the therapy of breast cancer. Synthesis and evaluation of estrogenic/antiestrogenic properties

Schertl, Sabine,Hartmann, Rolf W.,Batzl-Hartmann, Christine,Schlemmer, Richard,Spru, Thilo,Bernhardt, Guenther,Gust, Ronald,Schoenenberger, Helmut

, p. 125 - 137 (2007/10/03)

[meso-1,2-bis(2,6-dichloro-4-hydroxyphenyl)ethylenediamine]platinum(II) complexes (meso-1-ptll′; L,l′= Cl orL = H2O and L′ = OSO3) are highly effective towards hormone-sensitive, rodent breast cancers due to their significant estroge

Fullerene tectonics. Part 2. Synthesis and pyrolysis of halogenated benzo[c]phenanthrenes

Plater, M. John

, p. 2903 - 2909 (2007/10/03)

Halogenated benzo[c]phenanthrenes with a halogen in the hindered fiord region are prepared by the photochemical cyclisation of appropriately substituted stilbenes. Pyrolysis gives the corresponding benzo[ghi]fluoranthrenes in moderate yields. At higher temperatures a competing rearrangement pathway to cyclopenta[cd]pyrene occurs.

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