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Ethyl 4-bromocrotonate is a clear yellow liquid that serves as a crucial raw material and intermediate in various chemical processes. It is widely recognized for its applications in organic synthesis, pharmaceuticals, agrochemicals, and the dyestuffs industry.

37746-78-4

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37746-78-4 Usage

Uses

Used in Organic Synthesis:
Ethyl 4-bromocrotonate is used as a key intermediate for the synthesis of various organic compounds. Its chemical properties make it a versatile building block in the creation of complex molecules and structures.
Used in Pharmaceuticals:
In the pharmaceutical industry, Ethyl 4-bromocrotonate is utilized as a starting material for the development of new drugs. Its unique structure allows for the formation of various medicinal compounds with potential therapeutic applications.
Used in Agrochemicals:
Ethyl 4-bromocrotonate is employed as a vital component in the production of agrochemicals, such as pesticides and herbicides. Its role in these products contributes to the development of more effective and targeted solutions for agricultural needs.
Used in Dyestuffs:
In the dyestuffs industry, Ethyl 4-bromocrotonate is used as an intermediate for the synthesis of various dyes and pigments. Its chemical properties enable the creation of a wide range of colors and hues, catering to the diverse requirements of the textile and other related industries.

Check Digit Verification of cas no

The CAS Registry Mumber 37746-78-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,4 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 37746-78:
(7*3)+(6*7)+(5*7)+(4*4)+(3*6)+(2*7)+(1*8)=154
154 % 10 = 4
So 37746-78-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H9BrO2/c1-2-9-6(8)4-3-5-7/h3-4H,2,5H2,1H3/b4-3+

37746-78-4 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (A10371)  Ethyl 4-bromocrotonate, tech. 80%   

  • 37746-78-4

  • 10g

  • 239.0CNY

  • Detail
  • Alfa Aesar

  • (A10371)  Ethyl 4-bromocrotonate, tech. 80%   

  • 37746-78-4

  • 50g

  • 1081.0CNY

  • Detail
  • Alfa Aesar

  • (A10371)  Ethyl 4-bromocrotonate, tech. 80%   

  • 37746-78-4

  • 250g

  • 4715.0CNY

  • Detail

37746-78-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4-Bromocrotonate

1.2 Other means of identification

Product number -
Other names 2-Butenoic acid, 4-bromo-, ethyl ester, (E)-

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:37746-78-4 SDS

37746-78-4Relevant academic research and scientific papers

Stereoselective halo-succinimide mediated γ-halogenations of substituted α-trialkylsilyl-β,γ-unsaturated esters

Fealy, Lisa M.,Jennings, Michael P.

, (2020)

The halogenation of various α-ester allylsilanes with halo-succinimides (NXS, X = Cl, Br, and I) has been investigated. It has been shown that these reactions readily allow for good yields and excellent diastereoselectivities (up to >20:1) for a series of α-ester allylsilanes and halo-succinimide reagents, thereby providing a straightforward approach of preparing γ-halo-(E)-α,β-unsaturated esters.

FUNCTIONALIZED HETEROCYCLES AS ANTIVIRAL AGENTS

-

Paragraph 0395, (2020/04/10)

The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, thereof: which inhibit the protein(s) encoded by hepatitis B virus (HBV) or interfere with the function of the HBV life cycle of the hepatitis B virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HBV infection. The invention also relates to methods of treating an HBV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.

INHIBITORS OF BRUTON'S TYROSINE KINASE AND METHODS OF THEIR USE

-

Page/Page column 150, (2018/06/30)

Compounds of formula (I') and methods of their use and preparation, as well as compositions comprising compounds of formula (I').

INHIBITORS OF BRUTON'S TYROSINE KINASE AND METHODS OF THEIR USE

-

Page/Page column 150, (2017/09/02)

The present disclosure is directed to compounds of formula I and methods of their use and preparation, as well as compositions comprising compounds of formula I.

METHOD OF PREPARING AN ALKYLAMINE DERIVATIVE

-

, (2012/03/10)

The present invention provides a method of preparing an alkylamine derivates which hardly generates impurities and enables mass production with high purity.

Substituent-dictated partitioning of intermediates on the sulfide singlet oxygen reaction surface. A new mechanism for oxidative C-S bond cleavage in α-hydroperoxy sulfides

Toutchkine,Aebisher,Clennan

, p. 4966 - 4973 (2007/10/03)

The reactions of singlet oxygen with 17 sulfides bearing either anion or radical stabilizing substituents are reported. The abilities of substituents to modify product compositions in both the oxidative cleavage and sulfide oxidation pathways are analyzed in terms of partitioning of the hydroperoxy sulfonium ylide intermediate. Evidence is presented that suggests that the hydroperoxy sulfonium ylide exists in both diradical and zwitterionic forms. In addition, both inter- and intramolecular pathways for decomposition of α-hydroperoxy sulfides are suggested to rationalize the substituent-dependent formation of oxidative C-S bond cleavage products.

Piperdine and piperazine derivatives, and antihistaminic pharmaceutical compositions containing the same

-

, (2008/06/13)

Disclosed is a compound represented by Formula (I): STR1 wherein Ar1, Ar2, n, A, B and Z are as defined in claims. Disclosed are also a process for preparing the compound and pharmaceutical compositions containing the compound. The compound has an antihistamic and antiallergic effect.

Cyclopentane derivatives manufacture

-

, (2008/06/13)

The present invention relates to new cyclopentane derivatives having the formula STR1 and to a process for their manufacture. The compounds can be used as medicaments due to their antiprostaglandin effect.

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