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5-Phenyl-1H-1,2,3-triazole-4-carboxylic acid is a chemical compound with the molecular formula C10H7N3O2. It is a white crystalline solid that belongs to the class of 1,2,3-triazole derivatives, which are heterocyclic compounds containing a five-membered ring with three nitrogen atoms and two carbon atoms. This specific compound features a phenyl group (C6H5) attached to the 5-position of the triazole ring and a carboxylic acid group (-COOH) at the 4-position. It is synthesized through various chemical reactions and is used in the pharmaceutical and chemical industries for the development of new drugs, agrochemicals, and other applications. Due to its unique structure and properties, 5-Phenyl-1H-1,2,3-triazole-4-carboxylic acid has potential applications in various fields, including as a building block for the synthesis of more complex molecules and as a ligand in coordination chemistry.

830-78-4

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830-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 830-78-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 830-78:
(5*8)+(4*3)+(3*0)+(2*7)+(1*8)=74
74 % 10 = 4
So 830-78-4 is a valid CAS Registry Number.

830-78-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenyl-2H-triazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names HMS1697M17

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:830-78-4 SDS

830-78-4Downstream Products

830-78-4Relevant academic research and scientific papers

HETEROCYCLIC CARBOXYLATE COMPOUNDS AS GLYCOLATE OXIDASE INHIBITORS

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Page/Page column 105-106, (2021/05/07)

The present disclosure relates generally to modulators of human glycolate oxidase enzyme and methods of use and manufacture thereof. (I)

Fused v-Triazolo-heterocycles. Part 2. Synthesis of 4H-v-Triazolooxadiazin-4-ones from the 1-Aroylamino-v-triazole-5-carboxylic Acids

Rodios, Nestor A.

, p. 1275 - 1279 (2007/10/02)

The synthesis of some 4H-v-triazolooxadiazin-4-ones is described.They are prepared by the reaction of the corresponding 1-aroylamino-v-triazole-5-carboxylic acids with thionyl chloride in the presence of pyridine.The spectroscopic data of th

REACTION OF ACETYLENE NITRILES WITH AZIDES

Vereshchagin, L. I.,Filippova, T. M.,Bol'shedovorskaya, R. L.,Gavrilov, L. D.,Pavlova, G. A.

, p. 128 - 132 (2007/10/02)

The addition of organic and inorganic azides to 3-phenylpropynenitrile and 4-phenyl-2-hydroxy-3-butynenitrile was investigated.It was shown that organic azides add to 3-phenylpropynenitrile exclusively at the triple bond.The reaction with aluminum azide takes place with the participation of the acetylene bond and the nitrile group.The reaction of 4-phenyl-2-hydroxy-3-butynenitrile with azides is accompanied by decomposition to phenylpropargylaldehyde with the subsequent formation of 4-formyl-1,2,3-triazole.The oxidation of 4-phenyl-2-hydroxy-3-butynenitrile withactive manganese dioxide with the simultaneous addition of the azides leads to the formation of 4-carboxy-5-phenyl-1,2,3-triazole.

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