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19164-83-1

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19164-83-1 Usage

General Description

2,3-Bis-Bromomethyl-1,4-Dimethoxy-Benzene is a chemical compound that belongs to the group of bromomethyl- substituted aromatic compounds. It is commonly used in the synthesis of organic compounds and pharmaceuticals. 2,3-BIS-BROMOMETHYL-1,4-DIMETHOXY-BENZENE is a colorless liquid that is highly flammable and has a strong odor. It is mainly used as a reagent in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. 2,3-Bis-Bromomethyl-1,4-Dimethoxy-Benzene is also used in the manufacturing of dyes and as a solvent for polymerization reactions. However, it is important to handle this compound with care due to its flammability and toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 19164-83-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,6 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19164-83:
(7*1)+(6*9)+(5*1)+(4*6)+(3*4)+(2*8)+(1*3)=121
121 % 10 = 1
So 19164-83-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H12Br2O2/c1-13-9-3-4-10(14-2)8(6-12)7(9)5-11/h3-4H,5-6H2,1-2H3

19164-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-Bis(bromomethyl)-1,4-dimethoxybenzene

1.2 Other means of identification

Product number -
Other names 2,3-bis(bromomethyl)-1,4-dimethoxybenezene

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:19164-83-1 SDS

19164-83-1Relevant articles and documents

Bredow et al.

, p. 543,548,553 (1970)

Synthesis, X-ray structure and binding properties of molecular clips based on dimethylpropanediurea

Jansen, Rob J.,Rowan, Alan E.,De Gelder, Rene,Scheeren, Hans W.,Nolte, Roeland J. M.

, p. 121 - 122 (1998)

New concave host molecules show strong noncovalent binding of hydroxybenzene derivatives by an induced fit mechanism (Ka up to 3.4 × 106 dm3 mol-1).

Overriding Intrinsic Reactivity in Aliphatic C?H Oxidation: Preferential C3/C4 Oxidation of Aliphatic Ammonium Substrates

Heilmann, Michael,Knezevic, Melina,Piccini, Giovanni Maria,Tiefenbacher, Konrad

supporting information, p. 12387 - 12391 (2020/07/04)

The site-selective C?H oxidation of unactivated positions in aliphatic ammonium chains poses a tremendous synthetic challenge, for which a solution has not yet been found. Here, we report the preferential oxidation of the strongly deactivated C3/C4 positions of aliphatic ammonium substrates by employing a novel supramolecular catalyst. This chimeric catalyst was synthesized by linking the well-explored catalytic moiety Fe(pdp) to an alkyl ammonium binding molecular tweezer. The results highlight the vast potential of overriding the intrinsic reactivity in chemical reactions by guiding catalysis using supramolecular host structures that enable a precise orientation of the substrates.

Composition for treatment of pathogens that are resistant to tetracyclines

-

Paragraph 0105-0106, (2014/08/19)

The invention relates to compounds and pharmaceutical compositions useful in combination with tetracyclines in the treatment of bacterial infections caused by Gram-positive and Gram-negative pathogens, with particular efficacy in tetracycline resistant st

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