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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)-

4-bromo-7-methyl-1H-indole

Brc1ccc(c2c1cc[nH]2)C Request for Quotation
Chemical Name: 4-bromo-7-methyl-1H-indole
CAS Number: 936092-87-4
Product Number: AG00GRH5(AGN-PC-04Q611)
Synonyms:
MDL No: MFCD08272256
Molecular Formula: C9H8BrN
Molecular Weight: 210.0705

Identification/Properties

Computed Properties
Molecular Weight:
210.074g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
0
Exact Mass:
208.984g/mol
Monoisotopic Mass:
208.984g/mol
Topological Polar Surface Area:
15.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
149
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-H317
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Bromo-7-methyl-1H-indole, a versatile compound utilized in chemical synthesis, is a powerful building block in the pharmaceutical and agrochemical industries. This heterocyclic compound serves as a key intermediate in the synthesis of various bioactive molecules, including pharmaceutical drugs and agricultural chemicals. With its unique structure and reactivity, 4-Bromo-7-methyl-1H-indole plays a crucial role in the creation of complex organic compounds through functional group manipulation and cyclization reactions. Its distinct properties make it an essential tool for chemists engaged in the development of novel compounds with potential therapeutic and agricultural applications.