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Z-2-Bromo-4,4,4-trifluorbutenoic acid, ethyl ester is a chemical compound with the molecular formula C6H8BrF3O2. It is a derivative of butenoic acid and is commonly used in the synthesis of pharmaceuticals and agrochemicals. As an ethyl ester, it is the product of the reaction between the acid group of 2-Bromo-4,4,4-trifluorbutenoic acid and ethyl alcohol. Z-2-Bromo-4,4,4-trifluorbutenoic acid, ethyl ester is often utilized as an intermediate in the production of various organic compounds, with applications in the fields of organic chemistry and material science. Due to its toxic nature, it is crucial to handle and store Z-2-Bromo-4,4,4-trifluorbutenoic acid, ethyl ester with care to minimize health risks.

136264-28-3

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136264-28-3 Usage

Uses

Used in Pharmaceutical Industry:
Z-2-Bromo-4,4,4-trifluorbutenoic acid, ethyl ester is used as a synthetic intermediate for the production of various pharmaceuticals. Its unique structure allows for the creation of new drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, Z-2-Bromo-4,4,4-trifluorbutenoic acid, ethyl ester serves as a key intermediate in the synthesis of pesticides and other agrochemicals. Its properties enable the development of effective compounds for crop protection and management.
Used in Organic Chemistry Research:
Z-2-Bromo-4,4,4-trifluorbutenoic acid, ethyl ester is utilized as a reagent and intermediate in various organic chemistry reactions. Its versatility in forming different chemical bonds makes it valuable for research and development in organic chemistry.
Used in Material Science:
In the field of material science, Z-2-Bromo-4,4,4-trifluorbutenoic acid, ethyl ester is employed in the synthesis of novel materials with specific properties. Its unique molecular structure contributes to the development of advanced materials for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 136264-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,6 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 136264-28:
(8*1)+(7*3)+(6*6)+(5*2)+(4*6)+(3*4)+(2*2)+(1*8)=123
123 % 10 = 3
So 136264-28-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H6BrF3O2/c1-2-12-5(11)4(7)3-6(8,9)10/h3H,2H2,1H3/b4-3-

136264-28-3SDS

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 2-bromo-4,4,4-trifluorobut-2-enoate

1.2 Other means of identification

Product number -
Other names (Z)-ethyl 2-benzamido-4,4-difluorobut-2-enoate

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:136264-28-3 SDS

136264-28-3Relevant academic research and scientific papers

Halogenation of Electron-Deficient Vicinal Substituted Alkenes: Regio- and Stereoselectivity

Zubkov, Ilya N.,Ushakov, Igor A.,Chipanina, Nina N.,Rulev, Alexander Yu.

, p. 4130 - 4133 (2020)

The halogenation of electron-deficient vicinal substituted alkenes leads mainly to the mixture of regio- and stereoisomers of monohalogenated derivatives. Their ratio depends on the stability of the intermediate anionic complex and is determined by proper

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