Phenol, 3-(1H-tetrazol-5-yl)-|96859-34-6,AngeneChemical

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-

O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]

Tris(dibenzylideneacetone)dipalladium

C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C

Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Phenol, 3-(1H-tetrazol-5-yl)-

Request for Quotation

Chemical Name:	Phenol, 3-(1H-tetrazol-5-yl)-
CAS Number:	96859-34-6
Product Number:	AG005SJ5(AGN-PC-0OOHBQ)
Synonyms:
MDL No:	MFCD06797247
Molecular Formula:	C7H6N4O
Molecular Weight:	162.1487

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
Customer Feedback

Identification/Properties

Properties

BP:

436°C at 760 mmHg

Storage:

2-8℃;Inert atmosphere;

Form:

Solid

Safety Information

GHS Pictogram:

Signal Word:

Warning

UN#:

N/A

Hazard Statements:

H315-H319-H335

Precautionary Statements:

P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Class:

N/A

Packing Group:

N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Quantity Required:*

Company Name:

Contact Person:*

Email:*

Tel:*

Country:*

Others:(Optional)

Verification Code:

Customer Feedback

Chemical Structure

3-(1H-Tetrazol-5-yl)phenol, commonly referred to as $name$, is a versatile and valuable compound in chemical synthesis. This compound serves as a key building block in various organic reactions, particularly in the pharmaceutical and materials science industries. One significant application of 3-(1H-Tetrazol-5-yl)phenol lies in its use as a precursor in the synthesis of bioactive compounds and pharmaceutical drugs. Its unique structure containing a tetrazole ring makes it a valuable intermediate for the construction of heterocyclic scaffolds, which are commonly found in a wide range of drugs. Moreover, the presence of the phenol group allows for further functionalization, enabling the introduction of specific functionalities required for target molecule synthesis.Additionally, 3-(1H-Tetrazol-5-yl)phenol is often employed in the preparation of coordination polymers and metal-organic frameworks (MOFs). These materials have gained significant attention for their diverse applications in gas storage, catalysis, and molecular sensing. The coordination chemistry of this compound with metal ions facilitates the formation of intricate supramolecular architectures with tunable properties, making it a valuable component in the design of functional materials.Furthermore, the reactivity of 3-(1H-Tetrazol-5-yl)phenol can be harnessed in the development of novel organic reactions and synthetic methodologies. Its participation in click chemistry and radical processes has been explored to access complex molecular structures efficiently. This versatility makes it a valuable tool for organic chemists seeking to innovate in the field of chemical synthesis.In summary, the application of 3-(1H-Tetrazol-5-yl)phenol in chemical synthesis spans a wide range of areas, from pharmaceuticals to materials science, showcasing its utility as a versatile building block with diverse synthetic capabilities.