What is the 5-Phenyltetrazole?

5-Phenyltetrazole is white to almost white crystalline powder, while it's Molecular Formula is C7H6N4. white to almost white crystalline powder 5-Phenyl-1H-tetrazole may be used as ligand in the solvothermal synthesis of 3D polyoxometalate-based silver coordination polymers. It was used in the synthesis of 5-phenyltetrazolate organolanthanide complexes. It was used to investigate the corrosion inhibition of copper in salt water.

What is the CAS number for 5-Phenyltetrazole?

The CAS number of 5-Phenyltetrazole is 18039-42-4.

What is the 5-Phenyltetrazole?

5-Phenyltetrazole is white to almost white crystalline powder, while it's Molecular Formula is C7H6N4. white to almost white crystalline powder 5-Phenyl-1H-tetrazole may be used as ligand in the solvothermal synthesis of 3D polyoxometalate-based silver coordination polymers. It was used in the synthesis of 5-phenyltetrazolate organolanthanide complexes. It was used to investigate the corrosion inhibition of copper in salt water.

What is the CAS number for 5-Phenyltetrazole?

The CAS number of 5-Phenyltetrazole is 18039-42-4.

18039-42-4

Product Name:5-Phenyltetrazole
Molecular Formula:C₇H₆N₄
Molecular Weight:146.151

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Product Details

Detail

Cas No： 18039-42-4
Molecular Formula： C₇H₆N₄
Appearance： white to almost white crystalline powder
Purity： 99%

Product Name	5-Phenyltetrazole
Alias	5-phenyl-1h-tetrazol
English
Molecular formula	C7H6N4
Molecular weight	146.15
CAS No	18039-42-4
EINECS	241-950-8
Specification	Assay: 98%；99.0%. Melting point: 214-216℃ Moisture content：≦0.2%
Appearance traits	White crystal powder
Use	The intermediates of angiotensinase inhibitors.
Package	according to customer's requirement
Other product information

Factory supply 5-Phenyltetrazole 18039-42-4 (PTZ) with low price

Molecular Formula:C7H6N4
Molecular Weight:146.151
Appearance/Colour:white to almost white crystalline powder
Vapor Pressure:0.000165mmHg at 25°C
Melting Point:216 °C (dec.)(lit.)
Refractive Index:1.6530 (estimate)
Boiling Point:330.5 °C at 760 mmHg
PKA:4.28±0.10(Predicted)
Flash Point:161.3 °C
PSA：54.46000
Density:1.296 g/cm³
LogP:0.86670

5-Phenyltetrazole(Cas 18039-42-4) Usage

Synthesis	5-Phenyltetrazole can be prepared by reacting benzonitrile with hydrazine or hydrazine salt, and then reacting with nitrous acid.
Synthesis Reference(s)	Journal of the American Chemical Society, 80, p. 3908, 1958 DOI: 10.1021/ja01548a028Tetrahedron Letters, 38, p. 1257, 1997 DOI: 10.1016/S0040-4039(97)00052-XTetrahedron, 51, p. 11737, 1995 DOI: 10.1016/0040-4020(95)00725-N
General Description	Nucleophilic substitution reactions on 1,4-dimethoxybenzene and 1,3,5-trimethoxybenzene by the anions of 5-phenyl-1H-tetrazole has been investigated by paired electrosynthesis.

InChI:InChI=1/C7H5N4/c1-2-4-6(5-3-1)7-8-10-11-9-7/h1-5H/q-1

Our main markets are China, the United States, Europe, Korea, and Japan. The main business scope includes electronic chemicals, liquid crystal intermediates, high-purity metal compounds, pharmaceutical intermediates, special chemicals, and so on.

18039-42-4 Relevant articles

Tetrazoles: XLV. Amidoalkylation of 5-Substituted Tetrazoles

Myznikov,Esikov,Artamonova,Koldobskii

, p. 731 - 734 (2003)

Amidoalkylation of 5-aryl(hetaryl)tetraz...

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McMulkin, Calum J.,Massi, Massimiliano,Jones, Franca

, p. 2675 - 2681 (2015)

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Self-healing and moldable material with the deformation recovery ability from self-assembled supramolecular metallogels

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, p. 12847 - 12850 (2014)

A self-assembled non-covalent metallogel...

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Washburne,Peterson

, p. 427 (1970)

Synthesis, characterization, and biological evaluation of oxadiazole derivatives bearing 5-phenyl-tetrazole as osteoclast differentiation inhibitors

Moon, Seong-Hee,Latif, Muhammad,Qasim, Muhammad,Choi, Sik-Won,Lee, Joo Yun,Byun, Byung Jin,Saeed, Aamer,Kim, Seong Hwan

, p. 2247 - 2253 (2015)

Novel oxadiazoles bearing 5-phenyl-tetra...

Non-catalyzed addition of heterocyclic thiols and 5-substituted-1H-tetrazoles to vinyl ethers

Melnikova, Iuliia,Roh, Jaroslav,Kune?, Ji?í,Artamonova, Tatiana,Zevatskii, Yuri,Myznikov, Leonid

, p. 3842 - 3845 (2017)

The alkylation of 1-substituted 1H-tetra...

Investigation of N-[(acyloxy)alkyl] ester as a prodrug model for drugs containing the phenyltetrazole moiety

Alexander,Renyer,Rork

, p. 893 - 897 (1994)

N-Acyloxyalkylation using 5-phenyltetraz...

A novel route for the synthesis of 5-substituted 1-: H tetrazoles in the presence of polymer-supported palladium nanoparticles

Darbandizadeh Mohammad Abadi, Seyed Shahab Addin,Karimi Zarchi, Mohammad Ali

, p. 10397 - 10406 (2017)

A novel method for the synthesis of 5-su...

Efficient synthesis of tetrazole hemiaminal silyl ethers via three-component hemiaminal silylation

Xie, Ming-Sheng,Cheng, Xuan,Chen, Yang-Guang,Wu, Xiao-Xia,Qu, Gui-Rong,Guo, Hai-Ming

, p. 6890 - 6894 (2018)

An efficient route to construct 2,5-disu...

Dendron-functionalized Fe3O4 magnetic nanoparticles with palladium catalyzed CN insertion of arylhalide for the synthesis of tetrazoles and benzamide

Karimi Zarchi, Mohammad Ali,Darbandizadeh Mohammad Abadi, Seyed Shahab Addin

, p. 196 - 212 (2019)

A novel method for the one-pot synthesis...

An Expeditious Approach to Tetrazoles from Amides Utilizing Phosphorazidates

Ishihara, Kotaro,Shioiri, Takayuki,Matsugi, Masato

, p. 6244 - 6247 (2020)

A novel method was developed for the syn...

1-Disulfo-[2,2-bipyridine]-1,1-diium chloride ionic liquid as an efficient catalyst for the green synthesis of 5-substituted 1H-tetrazoles

Aali, Elaheh,Gholizadeh, Mostafa,Noroozi-Shad, Nazanin

, (2021/08/30)

A simple, green and efficient method has...

Sustainable and recyclable magnetic nanocatalyst of 1,10-phenanthroline Pd(0) complex in green synthesis of biaryls and tetrazoles using arylboronic acids as versatile substrates

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, (2021/04/02)

A magnetic nanocatalyst was purveyed as ...

Oxidation/ MCR domino protocol for direct transformation of methyl benzene, alcohol, and nitro compounds to the corresponding tetrazole using a three-functional redox catalytic system bearing TEMPO/Co(III)-porphyrin/ Ni(II) complex

Mahmoudi, Boshra,Rostami, Amin,Kazemnejadi, Milad,Hamah-Ameen, Baram Ahmed

, (2020/12/21)

A redox catalytic system for oxidation-r...

The anchoring of a Cu(ii)-salophen complex on magnetic mesoporous cellulose nanofibers: green synthesis and an investigation of its catalytic role in tetrazole reactions through a facile one-pot route

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, p. 19203 - 19220 (2021/06/03)

Today, most synthetic methods are aimed ...

18039-42-4 Process route

: 825-60-5
benzimidic acid ethyl ester

: 18039-42-4,3999-10-8
5-Phenyl-1H-tetrazole

Conditions

Conditions	Yield
With tris-(2-chloro-ethyl)-amine; benzene;
Multi-step reaction with 2 steps 1: hydrazine hydrate 2: nitric acid; sodium nitrite With nitric acid; hydrazine hydrate; sodium nitrite;

: 55513-24-1
1-hydroxy-5-phenyltetrazole

: 762-42-5
dimethyl acetylenedicarboxylate

: 18039-42-4,3999-10-8
5-Phenyl-1H-tetrazole

: 124313-67-3
dimethyl 5-phenyl-1-tetrazolyloxy-1,2-ethylenedicarboxylate (Z)

: 124313-68-4
dimethyl 5-phenyl-1-tetrazolyloxy-1,2-ethylenedicarboxylate (E)