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169610-52-0

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169610-52-0 Usage

General Description

2,6-Dimethoxybenzylbromide, also known as DMBr, is a chemical compound with the molecular formula C9H11BrO2. It is a colorless to pale yellow liquid with a strong, pungent odor. DMBr is commonly used as a reagent in organic synthesis to introduce the 2,6-dimethoxybenzyl (DMB) protecting group onto various functional groups. This chemical is important in the field of medicinal chemistry, as it can be used to protect hydroxyl and amine groups in pharmaceutical compounds, preventing them from undergoing unwanted reactions during synthesis. DMBr is also a key intermediate in the production of other organic chemicals and is commonly used in academic and industrial research laboratories. However, it should be handled with caution as it is a hazardous substance and can cause irritation to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 169610-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,6,1 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 169610-52:
(8*1)+(7*6)+(6*9)+(5*6)+(4*1)+(3*0)+(2*5)+(1*2)=150
150 % 10 = 0
So 169610-52-0 is a valid CAS Registry Number.

169610-52-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(bromomethyl)-1,3-dimethoxybenzene

1.2 Other means of identification

Product number -
Other names Benzene,2-(bromomethyl)-1,3-dimethoxy

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:169610-52-0 SDS

169610-52-0Relevant articles and documents

MLKL INHIBITORS

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Paragraph 0368-0369, (2018/09/26)

Purine derivatives that inhibit cellular necroptosis and/or human MLKL, pharmaceutical compositions thereof, and methods of treating an MLKL-mediated disorder with an effective amount of the compound or composition. Said MLKL-mediated disorder is pathology associated necroptosis, including ischemia-reperfusion damage, neurodegeneration, and inflammatory diseases such as acute pancreatitis, multiple sclerosis, inflammatory bowel disease, and allergic colitis.

Effect of methoxy substituents on the excited state properties of stilbene

Shinohara, Yoshihiro,Arai, Tatsuo

experimental part, p. 1500 - 1504 (2009/05/06)

Excited state properties of stilbenes having methoxy substituents at the ortho position of the phenyl ring have been studied and the remarkable methoxy substituent effect to suppress the fluorescence quantum yield depending on the number of methoxy substi

Insecticidal N-(substituted arylmethyl)-4-[bis(substituted phenyl)methyl]piperidines

-

, (2008/06/13)

Compounds of the following structure, the corresponding N-oxides and agriculturally acceptable salts, are disclosed as effective insecticides: STR1 in which U is selected from --(CH2)n -- and ethylidene; Q is selected from hydrogen, hydroxy, sulfhydryl, and fluorine; R is STR2 in which V is selected from hydrogen, halogen, alkyl, haloalkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsilyloxy, dialkylamino, cyano, nitro, hydroxy, and phenyl; Y and Z are independently selected from hydrogen and alkoxy; W and X taken together is --OCH2 CH2 O--, --CH2 C(CH3)2 O--, --OC(CH3)2 O--, or --N=C(C2 H5)O--; R1 and R2 are independently selected from phenyl substituted with halogen, alkyl, haloalkyl, haloalkoxy, alkoxyalkyl, hydroxy, arylthio, alkoxy, dialkylamino, dialkylaminosulfonyl, hydroxyalkylaminocarbonyl, alkylsulfonyloxy, and haloalkylsulfonyloxy; and n is 1, 2, or 3.

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