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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)-

Cyclopent[b]indole, 7-bromo-1,2,3,4-tetrahydro-

Brc1ccc2c(c1)c1CCCc1[nH]2 Request for Quotation
Chemical Name: Cyclopent[b]indole, 7-bromo-1,2,3,4-tetrahydro-
CAS Number: 164736-47-4
Product Number: AG001V35(AGN-PC-0JV4WR)
Synonyms:
MDL No:
Molecular Formula: C11H10BrN
Molecular Weight: 236.1078

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
236.112g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
0
Exact Mass:
235g/mol
Monoisotopic Mass:
235g/mol
Topological Polar Surface Area:
15.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
206
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Bromo-1,2,3,4-tetrahydrocyclopenta[b]indole is a versatile compound extensively used in chemical synthesis due to its unique structure and reactivity. It serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and functional materials. This compound acts as a valuable intermediate in the synthesis of indole derivatives, which are prevalent in medicinal chemistry and drug development. Its bromine substituent enables selective functionalization reactions, facilitating the introduction of diverse chemical groups for molecular modification. Furthermore, the tetrahydrocyclopenta[b]indole framework confers conformational rigidity, enhancing the structural diversity and biological activity of the final products. In organic synthesis, 7-Bromo-1,2,3,4-tetrahydrocyclopenta[b]indole demonstrates remarkable versatility and utility, making it an indispensable tool for creating novel compounds with potential applications in various fields.