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5-PHENYL-4-ISOXAZOLECARBOXYLIC ACID is a heterocyclic carboxylic acid with the molecular formula C10H7NO3. It features a five-membered isoxazole ring fused with a phenyl group, making it a versatile chemical compound. 5-PHENYL-4-ISOXAZOLECARBOXYLIC ACID is known for its potential as a building block in the synthesis of pharmaceuticals and agrochemicals, and it is valued for its structural and chemical properties that may also find applications in organic synthesis as a reagent or catalyst.

76344-95-1

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76344-95-1 Usage

Uses

Used in Pharmaceutical Industry:
5-PHENYL-4-ISOXAZOLECARBOXYLIC ACID is used as a drug intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new medications, contributing to the advancement of healthcare and treatment options.
Used in Agrochemical Industry:
In the agrochemical sector, 5-PHENYL-4-ISOXAZOLECARBOXYLIC ACID serves as a building block in the creation of agrochemicals. Its incorporation can lead to the development of more effective pesticides, herbicides, and other agricultural chemicals that enhance crop protection and yield.
Used in Organic Synthesis:
5-PHENYL-4-ISOXAZOLECARBOXYLIC ACID is utilized as a reagent in organic synthesis. Its chemical properties make it a valuable asset in the synthesis of complex organic compounds, facilitating reactions that may otherwise be challenging to achieve.
Used as a Catalyst in Chemical Reactions:
Due to its structural features, 5-PHENYL-4-ISOXAZOLECARBOXYLIC ACID may also function as a catalyst in certain chemical reactions. Its ability to increase the rate of reactions without being consumed in the process can improve the efficiency of various chemical processes and the synthesis of new chemical entities for medicinal purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 76344-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,4 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76344-95:
(7*7)+(6*6)+(5*3)+(4*4)+(3*4)+(2*9)+(1*5)=151
151 % 10 = 1
So 76344-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H7NO3/c12-10(13)8-6-11-14-9(8)7-4-2-1-3-5-7/h1-6H,(H,12,13)

76344-95-1 Well-known Company Product Price

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  • Aldrich

  • (633682)  5-Phenylisoxazole-4-carboxylicacid  97%

  • 76344-95-1

  • 633682-1G

  • 2,155.14CNY

  • Detail
  • Aldrich

  • (633682)  5-Phenylisoxazole-4-carboxylicacid  97%

  • 76344-95-1

  • 633682-5G

  • 7,499.70CNY

  • Detail

76344-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenyl-1,2-oxazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-phenylisoxazol-4-carboxylic acid

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:76344-95-1 SDS

76344-95-1Relevant academic research and scientific papers

A general and efficient PIFA mediated synthesis of heterocycle-fused quinolinone derivatives

Herrero, M.Teresa,Tellitu, Imanol,Domínguez, Esther,Hernández, Susana,Moreno, Isabel,SanMartín, Raúl

, p. 8581 - 8589 (2007/10/03)

A new application of the hypervalent iodine reagent phenyliodine(III)bis(trifluoroacetate) (PIFA) has been developed for the construction of a series of N, O, S-containing heterocycle-fused quinolinone derivatives in a general and efficient way. An altern

Reaction of 2-Dimethylaminomethylene-1,3-diones with Dinucleophiles. X. Synthesis of 5-Substituted Ethyl or Methyl 4-Isoxazolecarboxylates and Methyl 4-(2,2-Dimethyl-1-oxopropyl)-5-isoxazolecarboxylate

Schenone, Pietro,Fossa, Paola,Menozzi, Giulia

, p. 453 - 457 (2007/10/02)

Reaction of ethyl or methyl 2-dimethylaminomethylene-3-oxoalkanoates with hydroxylamine hydrochloride in methanol solution afforded in high yields the relative esters of 5-substituted 4-isoxazolecarboxylic acids II.These esters were hydrolyzed generally with concentrated hydrochloric acid-acetic acid mixtures to the corresponding carboxylic acids in satisfactory yields.Ethyl or methyl esters II isomerized with sodium ethoxide or methoxide, respectively, to the corresponding esters or hemiesters of 2-cyano-3-oxoalkanoic acids generally in excellent to satisfactory yields.Reaction of methyl 5,5-dimethyl-3-dimethylaminomethylene-2,4-dioxohexanoate with hydroxylamine hydrochloride afforded in moderate yield methyl 4-(2,2-dimethyl-1-oxopropyl)-5-isoxazolecarboxylate, which was converted by acid hydrolysis as above to 4-t-butyl-4-hydroxyfuroisoxazol-6-(4H)-one.

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