1H-TETRAZOLE, 1-PHENYL-

C1=NN=NN1C2=CC=CC=C2

InChIKey=IYPXPGSELZFFMI-UHFFFAOYSA-N

InChI=1S/C7H6N4/c1-2-4-7(5-3-1)11-6-8-9-10-11/h1-6H

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
Efficient alkene synthesis on solid support using the Julia-Kocienski coupling.	2010-11	20401532
Fluorinated 1-phenyl-1H-tetrazol-5-yl sulfone derivatives as general reagents for fluoroalkylidene synthesis.	2009-11-20	19831343
3,5-bis(trifluoromethyl)phenyl sulfones in the direct Julia-Kocienski olefination.	2005-08-05	16050703
An efficient synthesis of vinylsilanes from acylsilanes and alkyl 1-phenyl-1H-tetrazol-5-yl sulfones. Brook vs Smiles rearrangement.	2003-08-07	12889875

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:08:50 GMT 2025` Edited by `admin` on `Mon Mar 31 21:08:50 GMT 2025`
Record UNII	0LCC44M8Y9
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

1-PHENYL-1H-TETRAZOLE

Preferred Name

English

1H-TETRAZOLE, 1-PHENYL-

Systematic Name

English

Code System Code Type Description

CAS

5378-52-9

Created by admin on Mon Mar 31 21:08:50 GMT 2025 , Edited by admin on Mon Mar 31 21:08:50 GMT 2025

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FDA UNII

0LCC44M8Y9

Created by admin on Mon Mar 31 21:08:50 GMT 2025 , Edited by admin on Mon Mar 31 21:08:50 GMT 2025

PRIMARY

PUBCHEM

138477

Created by admin on Mon Mar 31 21:08:50 GMT 2025 , Edited by admin on Mon Mar 31 21:08:50 GMT 2025

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EPA CompTox

DTXSID6046765

Created by admin on Mon Mar 31 21:08:50 GMT 2025 , Edited by admin on Mon Mar 31 21:08:50 GMT 2025

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