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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
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)-

5-(4-Fluorophenethylsulfonyl)-1-phenyl-1H-tetrazole

Fc1ccc(cc1)CCS(=O)(=O)c1nnnn1c1ccccc1 Request for Quotation
Chemical Name: 5-(4-Fluorophenethylsulfonyl)-1-phenyl-1H-tetrazole
CAS Number: 1370411-43-0
Product Number: AG0012QQ(AGN-PC-0WAAS4)
Synonyms:
MDL No:
Molecular Formula: C15H13FN4O2S
Molecular Weight: 332.3527

Identification/Properties

Computed Properties
Molecular Weight:
332.353g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
5
Exact Mass:
332.074g/mol
Monoisotopic Mass:
332.074g/mol
Topological Polar Surface Area:
86.1A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
470
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(4-Fluorophenethylsulfonyl)-1-phenyl-1H-tetrazole is a versatile compound that finds wide application in chemical synthesis due to its unique structural properties. With its sulfonyl and tetrazole groups, this compound serves as a valuable building block in the synthesis of novel pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 5-(4-Fluorophenethylsulfonyl)-1-phenyl-1H-tetrazole is often employed as a key intermediate in the preparation of biologically active compounds. Its ability to undergo various transformations, such as substitution reactions and cyclization processes, makes it a valuable tool for organic chemists seeking to introduce specific functionalities into target molecules.Furthermore, the presence of the tetrazole moiety in this compound imparts unique properties that are beneficial for drug discovery and development. Tetrazole-containing compounds have been found to exhibit diverse biological activities, including antimicrobial, antiviral, and anticancer properties. Therefore, by using 5-(4-Fluorophenethylsulfonyl)-1-phenyl-1H-tetrazole as a starting material, researchers can access a wide range of structurally diverse molecules with potential pharmacological relevance.Overall, the application of 5-(4-Fluorophenethylsulfonyl)-1-phenyl-1H-tetrazole in chemical synthesis offers synthetic chemists a valuable tool for the efficient construction of complex molecules with diverse functionalities and potential biological activities.