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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-Indol-1-amine, 2,3-dihydro-2-methyl-, hydrochloride

NN1C(C)Cc2c1cccc2.Cl Request for Quotation
Chemical Name: 1H-Indol-1-amine, 2,3-dihydro-2-methyl-, hydrochloride
CAS Number: 102789-79-7
Product Number: AG003834(AGN-PC-0KK8N8)
Synonyms:
MDL No:
Molecular Formula: C9H13ClN2
Molecular Weight: 184.6659

Identification/Properties

Computed Properties
Molecular Weight:
184.667g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
184.077g/mol
Monoisotopic Mass:
184.077g/mol
Topological Polar Surface Area:
29.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
147
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methylindolin-1-amine hydrochloride, commonly known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and functional materials due to its unique structural properties.One prominent application of 2-Methylindolin-1-amine hydrochloride is in the pharmaceutical industry, where it is utilized for the synthesis of novel drug candidates. Its nitrogen-containing heterocyclic ring structure makes it a valuable scaffold for designing bioactive compounds with diverse biological activities.In addition, 2-Methylindolin-1-amine hydrochloride is utilized in the synthesis of specialty chemicals and advanced materials. Its presence in the chemical synthesis process contributes to the development of functional molecules with tailored properties for specific applications.Overall, the versatile nature of 2-Methylindolin-1-amine hydrochloride makes it a valuable tool in the hands of synthetic chemists for the creation of innovative compounds with potential implications in various industries.