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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-Indole, 5-iodo-

Ic1ccc2c(c1)cc[nH]2 Request for Quotation
Chemical Name: 1H-Indole, 5-iodo-
CAS Number: 16066-91-4
Product Number: AG001S3L(AGN-PC-0KL1KT)
Synonyms:
MDL No: MFCD00220065
Molecular Formula: C8H6IN
Molecular Weight: 243.0444

Identification/Properties

Properties
MP:
101-104 °C
BP:
341.7°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Stability:
Light Sensitive
Computed Properties
Molecular Weight:
243.047g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
0
Exact Mass:
242.954g/mol
Monoisotopic Mass:
242.954g/mol
Topological Polar Surface Area:
15.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
126
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:
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


The 5-Iodo-1H-indole is a versatile chemical compound widely used in organic synthesis. One of its primary applications lies in the field of medicinal chemistry, where it serves as a key building block for the synthesis of various pharmaceuticals and bioactive molecules. The 5-Iodo-1H-indole's unique structure provides a valuable platform for the introduction of functional groups and modifications, making it a valuable tool for chemical transformations. Additionally, this compound is utilized in the preparation of advanced materials and specialty chemicals, showcasing its importance in diverse areas of chemical research and development.