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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)-

2-Thiophenemethanamine,4-methyl-

Cc1cc(sc1)CN Request for Quotation
Chemical Name: 2-Thiophenemethanamine,4-methyl-
CAS Number: 104163-39-5
Product Number: AG008TYD(AGN-PC-0OSYMP)
Synonyms:
MDL No:
Molecular Formula: C6H9NS
Molecular Weight: 127.2074

Identification/Properties

Computed Properties
Molecular Weight:
127.205g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
127.046g/mol
Monoisotopic Mass:
127.046g/mol
Topological Polar Surface Area:
54.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
74.9
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(4-Methylthiophen-2-yl)methanamine is a versatile organic compound widely utilized in chemical synthesis due to its unique properties and reactivity. As a primary amine, it serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and advanced materials. The presence of a thienyl moiety enhances its utility in heterocyclic chemistry, allowing for the synthesis of complex structures with potential biological activities. Additionally, the methyl substituent provides steric effects that can influence the direction of chemical reactions, making this compound a valuable tool in the design and development of new molecules. Its compatibility with a variety of functional groups further expands its synthetic applications, enabling chemists to access a diverse array of molecular architectures with tailored properties.