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1260029-44-4

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1260029-44-4 Usage

Description

(E)-4-(2,4,5-trifluoro-phenyl)-but-2-enoic acid methyl ester is a chemical compound with the molecular formula C11H9F3O2. It is a methyl ester derivative of butenoic acid, featuring a unique trifluorophenyl group that contributes to its distinct properties and applications.

Uses

Used in Organic Synthesis:
(E)-4-(2,4,5-trifluoro-phenyl)-but-2-enoic acid methyl ester is used as a reagent in organic synthesis for the creation of various drug compounds and agrochemicals. Its trifluorophenyl group enhances the biological and pharmacokinetic properties of potential drug candidates, making it a valuable building block in the development of new molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (E)-4-(2,4,5-trifluoro-phenyl)-but-2-enoic acid methyl ester serves as a key building block for the synthesis of drug compounds. Its unique structural features allow researchers to modify and optimize the properties of drug candidates, potentially leading to more effective and safer medications.
Used as a Reference Standard in Analytical Chemistry:
(E)-4-(2,4,5-trifluoro-phenyl)-but-2-enoic acid methyl ester is also utilized as a reference standard in analytical chemistry. It aids in the identification and quantification of (E)-4-(2,4,5-trifluoro-phenyl)-but-2-enoic acid and related compounds in various samples, ensuring accurate and reliable results in chemical analysis.

Check Digit Verification of cas no

The CAS Registry Mumber 1260029-44-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,0,2 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1260029-44:
(9*1)+(8*2)+(7*6)+(6*0)+(5*0)+(4*2)+(3*9)+(2*4)+(1*4)=114
114 % 10 = 4
So 1260029-44-4 is a valid CAS Registry Number.

1260029-44-4Relevant articles and documents

Cobalt-Catalyzed Cross-Coupling of Grignards with Allylic and Vinylic Bromides: Use of Sarcosine as a Natural Ligand

Frlan, Rok,Sova, Matej,Gobec, Stanislav,Stavber, Gaj,?asar, Zdenko

, p. 7803 - 7809 (2015/08/18)

Sarcosine was discovered to be an excellent ligand for cobalt-catalyzed carbon-carbon cross-coupling of Grignard reagents with allylic and vinylic bromides. The Co(II)/sarcosine catalytic system is shown to perform efficiently when phenyl and benzyl Grignards are coupled with alkenyl bromides. Notably, previously unachievable Co-catalyzed coupling of allylic bromides with Grignards to linearly coupled α-products was also realized with Co(II)/sarcosine catalyst. This method was used for efficient preparation of the key intermediate in an alternative synthesis of the antihyperglycemic drug sitagliptin.

PREPARATION OF SITAGLIPTIN INTERMEDIATES

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Paragraph 0275; 0276, (2014/07/08)

The invention relates to the preparation of chiral compounds, in particular to the preparation of chiral compounds which may be used as intermediates for the preparation of anti-diabetic agents, preferably sitagliptin.

PREPARATION OF SITAGLIPTIN INTERMEDIATES

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Page/Page column 20, (2013/02/28)

The invention relates to the preparation of chiral compounds, in particular to the preparation of chiral compounds which may be used as intermediates for the preparation of anti-diabetic agents, preferably sitagliptin.

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