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21969-32-4

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21969-32-4 Usage

Chemical Properties

Brown liquid

Uses

1-Methyl-2-propenylmagnesium chloride is a Grignard type allylating reagent that can be used for the preparation of corresponding homoallylic alcohols by reacting with various aldehydes. It can also be utilized in the synthesis of 3,4-dihydro-4-(1-methyl-2-propen-1-yl)-2(1H)-pyrimidinethione derivatives by treating with 2-mercaptopyrimidine.

Check Digit Verification of cas no

The CAS Registry Mumber 21969-32-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,6 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21969-32:
(7*2)+(6*1)+(5*9)+(4*6)+(3*9)+(2*3)+(1*2)=124
124 % 10 = 4
So 21969-32-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H7.ClH.Mg/c1-3-4-2;;/h3-4H,1H2,2H3;1H;/q;;+1/p-1/rC4H7ClMg/c1-3-4(2)6-5/h3-4H,1H2,2H3

21969-32-4 Well-known Company Product Price

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  • Aldrich

  • (420042)  1-Methyl-2-propenylmagnesiumchloridesolution  0.5 M in THF

  • 21969-32-4

  • 420042-100ML

  • 659.88CNY

  • Detail

21969-32-4SDS

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 magnesium,but-1-ene,chloride

1.2 Other means of identification

Product number -
Other names chlorure de buten-2 ylmagnesium

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:21969-32-4 SDS

21969-32-4Upstream product

21969-32-4Relevant articles and documents

Process for preparing 1-bromoalkylbenzene derivatives and intermediates thereof

-

, (2008/06/13)

A 1-bromoalkylbenzene derivative is prepared by reacting a phenylalkene derivative with hydrogen bromide in the presence of a non-polar solvent. The phenylalkene derivative is prepared by reacting an alkenyl halide with metal magnesium to form a Grignard reagent, and then reacting the Grignard reagent with a benzyl halide derivative. An allyl Grignard reagent is prepared by reacting continuously an allyl halide derivative with metal magnesium in an organic solvent, in which the allyl halide derivative and metal magnesium are continuously added to the reaction system and the allyl Grignard reagent formed is continuously removed from the reaction system. The processes provide the intended compounds in high yields, high selectivities and high purities.

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