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308796-07-8

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308796-07-8 Usage

Description

1-METHYLBUTYLZINC BROMIDE, also known as butylmethylzinc bromide, is an organozinc compound with the chemical formula C5H11BrZn. It is a colorless to light yellow liquid that is highly reactive, particularly towards water and air. 1-METHYLBUTYLZINC BROMIDE is commonly used in organic synthesis as a nucleophile in the Grignard reaction, which allows for the formation of carbon-carbon bonds. It can also be used in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, 1-METHYLBUTYLZINC BROMIDE has been studied for its unique reactivity and potential applications in the field of organic chemistry. Due to its high reactivity and potential hazards, this compound must be handled and stored with extreme caution.

Uses

Used in Organic Synthesis:
1-METHYLBUTYLZINC BROMIDE is used as a nucleophile in the Grignard reaction for the formation of carbon-carbon bonds. This reaction is a widely used method in organic synthesis for creating new carbon-carbon bonds, which is essential for the construction of complex organic molecules.
Used in Pharmaceutical Production:
1-METHYLBUTYLZINC BROMIDE is used as a reagent in the synthesis of pharmaceuticals for the development of new drugs and medicines. Its unique reactivity allows for the formation of specific carbon-carbon bonds that are crucial in the creation of bioactive compounds.
Used in Agrochemical Production:
1-METHYLBUTYLZINC BROMIDE is used as a reagent in the synthesis of agrochemicals for the development of new pesticides, herbicides, and other agricultural chemicals. Its application in this field contributes to the advancement of agricultural technology and crop protection.
Used in Fine Chemicals Production:
1-METHYLBUTYLZINC BROMIDE is used as a reagent in the synthesis of fine chemicals for various applications, including specialty chemicals, fragrances, and flavorings. Its unique reactivity allows for the creation of specific chemical structures that are important in these industries.
Used in Research and Development:
1-METHYLBUTYLZINC BROMIDE is used as a research compound in the field of organic chemistry to study its unique reactivity and explore potential applications. This research can lead to the discovery of new reactions and the development of innovative synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 308796-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,8,7,9 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 308796-07:
(8*3)+(7*0)+(6*8)+(5*7)+(4*9)+(3*6)+(2*0)+(1*7)=168
168 % 10 = 8
So 308796-07-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H11.BrH.Zn/c1-3-5-4-2;;/h3H,4-5H2,1-2H3;1H;/q;;+1/p-1/rC5H11BrZn/c1-3-4-5(2)7-6/h5H,3-4H2,1-2H3

308796-07-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H58078)  1-Methylbutylzinc bromide, 0.5M in THF, packaged under Argon in resealable ChemSeal? bottles   

  • 308796-07-8

  • 50ml

  • 1019.0CNY

  • Detail
  • Aldrich

  • (499269)  1-Methylbutylzincbromidesolution  0.5 M in THF

  • 308796-07-8

  • 499269-50ML

  • 968.76CNY

  • Detail

308796-07-8SDS

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 bromozinc(1+),pentane

1.2 Other means of identification

Product number -
Other names 1-Methylbutylzinc bromide solution

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:308796-07-8 SDS

308796-07-8Downstream Products

308796-07-8Relevant articles and documents

Pd-PEPPSI-IPentCl: A highly effective catalyst for the selective cross-coupling of secondary organozinc reagents

Pompeo, Matthew,Hadei, Niloufar,Organ, Michael G.,Froese, Robert D. J.

, p. 11354 - 11357,4 (2012/12/12)

No migration? No problem. A series of new N-heterocyclic carbene based Pd complexes has been created and evaluated in the Negishi cross-coupling of aryl and heteroaryl chlorides, bromides, and triflates with a variety of secondary alkylzinc reagents (see scheme). The direct elimination product is nearly exclusively formed; in most examples there is no migratory insertion at all. Copyright

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