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  2. 1H-1,2,4-Triazole, 1-[[2,4,6-tris(1-methylethyl)phenyl]sulfonyl]-

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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)-

1H-1,2,4-Triazole, 1-[[2,4,6-tris(1-methylethyl)phenyl]sulfonyl]-

CC(c1cc(cc(c1S(=O)(=O)n1cncn1)C(C)C)C(C)C)C Request for Quotation
Chemical Name: 1H-1,2,4-Triazole, 1-[[2,4,6-tris(1-methylethyl)phenyl]sulfonyl]-
CAS Number: 54230-60-3
Product Number: AG003B0V(AGN-PC-0JUYOH)
Synonyms:
MDL No:
Molecular Formula: C17H25N3O2S
Molecular Weight: 335.4643

Identification/Properties

Properties
MP:
111-114 °C
BP:
451.9°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Stability:
Moisture Sensitive
Computed Properties
Molecular Weight:
335.466g/mol
XLogP3:
4.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
335.167g/mol
Monoisotopic Mass:
335.167g/mol
Topological Polar Surface Area:
73.2A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
467
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#:
-
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-((2,4,6-Triisopropylphenyl)sulfonyl)-1H-1,2,4-triazole is a versatile chemical compound widely used in chemical synthesis processes. This compound serves as an excellent sulfonating agent in organic chemistry, enabling the introduction of sulfonyl functional groups to various organic molecules. The presence of the triisopropylphenyl moiety imparts sterically bulky properties to the molecule, making it particularly useful for selective sulfonation reactions.Additionally, 1-((2,4,6-Triisopropylphenyl)sulfonyl)-1H-1,2,4-triazole has found application as a protective group in organic synthesis. Its ability to mask reactive functional groups in a reversible manner allows chemists to control the reactivity of specific sites within a molecule during multi-step synthesis. This compound's stability under a wide range of reaction conditions makes it a valuable tool for protecting sensitive functional groups while allowing desired transformations to occur elsewhere.Moreover, 1-((2,4,6-Triisopropylphenyl)sulfonyl)-1H-1,2,4-triazole is instrumental in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its versatility and compatibility with various reaction protocols make it a staple reagent in the arsenal of synthetic chemists seeking to construct complex molecular structures efficiently and selectively.