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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-4-amine, 6-chloro-

Clc1cc(N)c2c(c1)[nH]cc2 Request for Quotation
Chemical Name: 1H-Indol-4-amine, 6-chloro-
CAS Number: 431046-15-0
Product Number: AG00DEHK(AGN-PC-01NGKQ)
Synonyms:
MDL No:
Molecular Formula: C8H7ClN2
Molecular Weight: 166.6076

Identification/Properties

Properties
BP:
394°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
166.608g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
166.03g/mol
Monoisotopic Mass:
166.03g/mol
Topological Polar Surface Area:
41.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
151
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-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


6-Chloro-1H-indol-4-amine, a key building block in organic chemistry, finds extensive application in chemical synthesis processes. This compound serves as a versatile intermediate for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structural properties, 6-Chloro-1H-indol-4-amine plays a crucial role in the development of biologically active compounds and complex organic molecules. Specifically, it is utilized in the synthesis of indole derivatives, which are known for their diverse pharmacological activities. By incorporating 6-Chloro-1H-indol-4-amine into synthetic routes, chemists can access a wide range of functionalized molecules with potential applications in drug discovery, material science, and other research areas. This compound's ability to undergo various transformations and form new carbon-carbon and carbon-nitrogen bonds makes it an indispensable tool for organic chemists seeking to design and prepare novel compounds with targeted properties.