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322640-05-1

3,5-DIMETHOXYPHENYLMAGNESIUM BROMIDE is a magnesium organometallic compound that is widely utilized in organic synthesis as a reagent for Grignard reactions. It is characterized by the presence of a bromide ion and a 3,5-dimethoxyphenyl group, which endows it with the capability to engage in reactions with a range of organic halides, ketones, and esters, facilitating the formation of new carbon-carbon bonds. 3,5-DIMETHOXYPHENYLMAGNESIUM BROMIDE is recognized for its versatility and significance in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, making it an indispensable tool in the field of organic chemistry.

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  • 322640-05-1 Structure

  • Basic information

    1. Product Name: 3,5-DIMETHOXYPHENYLMAGNESIUM BROMIDE
    2. Synonyms: 3,5-DIMETHOXYPHENYLMAGNESIUM BROMIDE
    3. CAS NO:322640-05-1
    4. Molecular Formula: C8H9BrMgO2
    5. Molecular Weight: 241.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 322640-05-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,5-DIMETHOXYPHENYLMAGNESIUM BROMIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-DIMETHOXYPHENYLMAGNESIUM BROMIDE(322640-05-1)
    11. EPA Substance Registry System: 3,5-DIMETHOXYPHENYLMAGNESIUM BROMIDE(322640-05-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 322640-05-1(Hazardous Substances Data)

322640-05-1 Usage

Uses

Used in Organic Synthesis:
3,5-DIMETHOXYPHENYLMAGNESIUM BROMIDE is used as a reagent in Grignard reactions for the formation of new carbon-carbon bonds. Its ability to react with various organic halides, ketones, and esters makes it a valuable tool in creating complex organic molecules.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 3,5-DIMETHOXYPHENYLMAGNESIUM BROMIDE is used as a key intermediate in the synthesis of various drugs. Its role in forming carbon-carbon bonds is crucial for the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Synthesis:
3,5-DIMETHOXYPHENYLMAGNESIUM BROMIDE is also utilized in the agrochemical sector as a reagent for the synthesis of agrochemicals. Its capacity to form new carbon-carbon bonds is essential in the creation of novel compounds with pesticidal or herbicidal properties.
Used in Fine Chemicals Synthesis:
In the synthesis of fine chemicals, 3,5-DIMETHOXYPHENYLMAGNESIUM BROMIDE is employed as a versatile reagent for the production of specialty chemicals. Its reactivity with a variety of organic compounds allows for the development of high-value chemical products used in various applications, such as fragrances, dyes, and other specialty materials.

Check Digit Verification of cas no

The CAS Registry Mumber 322640-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,2,6,4 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 322640-05:
(8*3)+(7*2)+(6*2)+(5*6)+(4*4)+(3*0)+(2*0)+(1*5)=101
101 % 10 = 1
So 322640-05-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H9O2.BrH.Mg/c1-9-7-4-3-5-8(6-7)10-2;;/h4-6H,1-2H3;1H;/q;;+1/p-1/rC8H9BrMgO2/c1-11-7-3-6(10-9)4-8(5-7)12-2/h3-5H,1-2H3

322640-05-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name magnesium,1,3-dimethoxybenzene-5-ide,bromide

1.2 Other means of identification

Product number -
Other names 3,5-Dimethoxyphenylmagnesium bromide 0.5 M in Tetrahydrofuran

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:322640-05-1 SDS

322640-05-1Relevant articles and documents

Chromium(II)-Catalyzed Diastereoselective and Chemoselective Csp2-Csp3 Cross-Couplings Using Organomagnesium Reagents

Li, Jie,Ren, Qianyi,Cheng, Xinyi,Karaghiosoff, Konstantin,Knochel, Paul

supporting information, p. 18127 - 18135 (2019/11/19)

A simple protocol for performing chromium-catalyzed highly diastereoselective alkylations of arylmagnesium halides with cyclohexyl iodides at ambient temperature has been developed. Furthermore, this ligand-free CrCl2 enables efficient electrophilic alkenylations of primary, secondary, and tetiary alkylmagnesium halides with readily available alkenyl acetates. Moreover, this chemoselective C-C coupling reaction with stereodefined alkenyl acetates proceeds in a stereoretentive fashion. A wide range of functional groups on alkyl iodides and alkenyl acetates are well tolerated, thus furnishing functionalized Csp2-Csp3 coupling products in good yields and high diastereoselectivity. Detailed mechanistic studies suggest that the in situ generated low-valent chromium(I) species might be the active catalyst for these Csp2-Csp3 cross-couplings.

QUINOLINES AS FGFR KINASE MODULATORS

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Page/Page column 159, (2013/05/21)

The invention relates to new quinoline derivative compounds of formula (I), to pharmaceutical compositions comprising said compounds, to processes for the preparation of said compounds and to the use of said compounds in the treatment of diseases, e.g. ca

Substituted heterocyclic compounds and uses thereof

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Page/Page column 43-44, (2008/06/13)

The present invention relates to substituted heterocyclic compounds and compositions comprising a substituted heterocyclic compound. The present invention also relates to methods for preventing or treating various diseases and disorders by administering t

NOVEL ANALGESIC AND IMMUNOMODULATORY CANNABINOIDS

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, (2008/06/13)

Disclosed are novel compounds represented by the following structural formula: R—X—Y; and physiologically acceptable salts thereof. R is a tricyclic core of a cannabinoid or substituted cannabinoid. X is a covalent bond, —CH2— or —CHR1—, wherei

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