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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)-

1,3,4-Thiadiazol-2-amine, 5-[4-(1,1-dimethylethyl)phenyl]-

CC(c1ccc(cc1)c1nnc(s1)N)(C)C Request for Quotation
Chemical Name: 1,3,4-Thiadiazol-2-amine, 5-[4-(1,1-dimethylethyl)phenyl]-
CAS Number: 100987-04-0
Product Number: AG0003DN(AGN-PC-0JWF6M)
Synonyms:
MDL No: MFCD00980739
Molecular Formula: C12H15N3S
Molecular Weight: 233.3326

Identification/Properties

Computed Properties
Molecular Weight:
233.333g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
233.099g/mol
Monoisotopic Mass:
233.099g/mol
Topological Polar Surface Area:
80A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
231
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(4-(tert-Butyl)phenyl)-1,3,4-thiadiazol-2-amine is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound is commonly used as a building block in the synthesis of various organic molecules due to its functional groups and structural features.In organic synthesis, 5-(4-(tert-Butyl)phenyl)-1,3,4-thiadiazol-2-amine serves as a valuable starting material for the creation of complex molecules with specific functionalities. Its amine group can undergo various reactions such as acylation, alkylation, and nucleophilic substitution, allowing for the introduction of different substituents or functional groups at this position.Furthermore, the thiadiazole ring in this compound provides opportunities for further chemical modifications, such as oxidation, reduction, or heterocyclic transformations, leading to the generation of novel compounds with diverse applications in medicinal chemistry, materials science, and agrochemicals.Overall, the application of 5-(4-(tert-Butyl)phenyl)-1,3,4-thiadiazol-2-amine in chemical synthesis enables the efficient and controlled construction of complex organic molecules, making it a valuable tool for researchers and chemists striving to develop new compounds with specific properties and functions.