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3-Methoxybenzylzinc chloride is a chemical compound that features a benzylzinc chloride group with a methoxy (CH3O) functional group attached at the para position of the benzene ring. It is a versatile reagent in organic synthesis, particularly for the formation of carbon-carbon bonds. 3-METHOXYBENZYLZINC CHLORIDE is highly valued in organic chemistry for its ability to engage in selective and efficient carbon-carbon bond formation, making it instrumental in the synthesis of a wide range of organic compounds.

312693-16-6

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312693-16-6 Usage

Uses

Used in Organic Synthesis:
3-Methoxybenzylzinc chloride is used as a reagent for the formation of carbon-carbon bonds, which is crucial in creating complex organic molecules. Its ability to form these bonds selectively and efficiently makes it a preferred choice in various organic synthesis processes.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 3-Methoxybenzylzinc chloride is used as a key intermediate in the synthesis of various pharmaceuticals. Its role in creating carbon-carbon bonds allows for the development of new and innovative drug molecules with potential therapeutic applications.
Used in Natural Product Synthesis:
3-Methoxybenzylzinc chloride is also utilized in the synthesis of natural products, which are often complex organic compounds derived from plants, animals, or microorganisms. Its ability to form carbon-carbon bonds is essential in replicating the intricate structures of these natural products for research and commercial purposes.
Used in Fine Chemicals Production:
In the production of fine chemicals, which are high-purity chemicals used in various industries, 3-Methoxybenzylzinc chloride serves as a valuable reagent. Its contribution to the formation of carbon-carbon bonds is vital for creating high-quality specialty chemicals used in applications such as fragrances, dyes, and agrochemicals.
Used in Grignard-Type Reactions:
3-Methoxybenzylzinc chloride is particularly useful in Grignard-type reactions, which are a class of chemical reactions that involve the formation of carbon-carbon bonds. Its application in these reactions contributes to the synthesis of a variety of organic compounds, showcasing its versatility and importance in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 312693-16-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,2,6,9 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 312693-16:
(8*3)+(7*1)+(6*2)+(5*6)+(4*9)+(3*3)+(2*1)+(1*6)=126
126 % 10 = 6
So 312693-16-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H9O.ClH.Zn/c1-7-4-3-5-8(6-7)9-2;;/h3-6H,1H2,2H3;1H;/q;;+1/p-1/rC8H9ClOZn/c1-10-8-4-2-3-7(5-8)6-11-9/h2-5H,6H2,1H3

312693-16-6 Well-known Company Product Price

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  • Aldrich

  • (498793)  3-Methoxybenzylzincchloridesolution  0.5 M in THF

  • 312693-16-6

  • 498793-50ML

  • 2,811.51CNY

  • Detail

312693-16-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name chlorozinc(1+),1-methanidyl-3-methoxybenzene

1.2 Other means of identification

Product number -
Other names 3-Methoxybenzylzinc chloride 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:312693-16-6 SDS

312693-16-6Relevant academic research and scientific papers

Asymmetric Synthesis of Fluorinated Allenes by Rhodium-Catalyzed Enantioselective Alkylation/Defluorination of Propargyl Difluorides with Alkylzincs

Hayashi, Tamio,Ng, Jia Sheng

supporting information, p. 20771 - 20775 (2021/08/25)

The reaction of propargyl difluorides R1CF2C≡CR2 with alkylzincs R3ZnCl giving axially chiral fluorinated allenes R1FC=C=CR2R3 with high enantioselectivity (up to 99 % ee) was found to be catalyzed by a chiral diene/rhodium complex. A key step in the catalytic cycle is selective elimination of one of the enantiotopic fluorides at the β-position of an alkenyl-Rh intermediate, which is generated by regioselective addition of R3-Rh onto the triple bond of the starting difluorides.

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