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122549-26-2

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122549-26-2 Usage

Description

(E/Z)-4-CARBOXYMETHYL-5-(4-FLUOROPHENYL)-2-METHYL-PENT-4-EN-3-ONE, with the CAS number 122549-26-2, is a light yellow oil compound that is useful in organic synthesis. It is characterized by its unique molecular structure, which includes a 4-carboxymethyl group, a 4-fluorophenyl group, and a 2-methylpent-4-en-3-one backbone.

Uses

Used in Organic Synthesis:
(E/Z)-4-CARBOXYMETHYL-5-(4-FLUOROPHENYL)-2-METHYL-PENT-4-EN-3-ONE is used as a synthetic intermediate for the production of various organic compounds. Its unique structure allows it to be a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (E/Z)-4-CARBOXYMETHYL-5-(4-FLUOROPHENYL)-2-METHYL-PENT-4-EN-3-ONE is used as a key intermediate in the synthesis of drug candidates. Its presence in the molecular structure can impart specific biological activities, making it a valuable component in the development of new medications.
Used in Agrochemical Industry:
(E/Z)-4-CARBOXYMETHYL-5-(4-FLUOROPHENYL)-2-METHYL-PENT-4-EN-3-ONE is also utilized in the agrochemical industry as a precursor for the synthesis of pesticides and other crop protection agents. Its unique properties can contribute to the development of more effective and targeted agrochemical products.
Used in Specialty Chemicals:
In the specialty chemicals sector, (E/Z)-4-CARBOXYMETHYL-5-(4-FLUOROPHENYL)-2-METHYL-PENT-4-EN-3-ONE is employed as a component in the production of various specialty chemicals, such as dyes, fragrances, and other high-value compounds. Its unique structure and properties make it a valuable asset in the synthesis of these complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 122549-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,5,4 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 122549-26:
(8*1)+(7*2)+(6*2)+(5*5)+(4*4)+(3*9)+(2*2)+(1*6)=112
112 % 10 = 2
So 122549-26-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H15FO3/c1-9(2)13(16)12(14(17)18-3)8-10-4-6-11(15)7-5-10/h4-9H,1-3H3/b12-8+

122549-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-fluorophenyl)methylene]-4-methyl-3-oxo-pentanoic acid methyl ester

1.2 Other means of identification

Product number -
Other names (E/Z)-4-Carboxymethyl-5-(4-fluorophenyl)-2-methyl-pent-4-en-3-one

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:122549-26-2 SDS

122549-26-2Relevant articles and documents

Method for continuously preparing rosuvastatin intermediate by micro-channel modular reaction device

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Page/Page column 9-14, (2019/06/27)

The invention discloses a method for continuously preparing a rosuvastatin intermediate by a micro-channel modular reaction device. The method includes the steps: performing reaction on isopropanol solution of fluorobenzaldehyde and isopropanol solution o

PREPARATION OF ALKYL 4-(4-FLUOROPHENYL)-6-ISOPROPYL-2-[METHYL(METHYLSULFONY)AMINO]-PYRIMIDINE-5-CARBOXYLATE AND ITS SUBSEQUENT CONVERSION TO N-[4-(4-FLUOROPHENYL)-5-FORMYL-6-ISOPROPYL PYRIMIDIN-2-YL]-N-METHYLMETHANESULFONAMIDE-A KEY INTERMEDIATE IN THE SYNTHESIS OF ROSUVASTATIN

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Page/Page column 13-14, (2008/06/13)

The present invention discloses a novel process to prepare a compound of formula (IIA). By reacting a compound of formula-[D], wherein R1 is C1 to C6 alkyl, preferably R1 is methyl or ethyl, more preferably R1 is methyl ; and R2 is C1 to C8 n-alkyl or branched alkyl, cycloalkyl, phenyl , benzyl or substituted phenyl group, preferably R2 is methyl ; with N-methyl methanesulfonamide and a base, optionally with a salt of N-methyl methanesulfonamide, in suitable solvent(s) , to give a compound of formula (IIA), followed by converting compound of formula (IIA) to a compound for formula -[B], by a known process and finally converting a compound of formula (B) to a compound of formula (II), by a novel process using calcium hypochlorite / TEMPO as an oxidant.

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