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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-2,3-dione, 5-bromo-6-methyl-

O=C1Nc2c(C1=O)cc(c(c2)C)Br Request for Quotation
Chemical Name: 1H-Indole-2,3-dione, 5-bromo-6-methyl-
CAS Number: 106976-23-2
Product Number: AG003MJS(AGN-PC-00O08T)
Synonyms:
MDL No:
Molecular Formula: C9H6BrNO2
Molecular Weight: 240.0534

Identification/Properties

Properties
MP:
200℃ (acetic acid )
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
240.056g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
238.958g/mol
Monoisotopic Mass:
238.958g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
266
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#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-6-methylindoline-2,3-dione is a versatile compound that finds wide application in chemical synthesis, particularly in the field of organic chemistry. This compound serves as a valuable building block for the creation of various complex organic molecules due to its unique structural properties and reactivity. In chemical synthesis, 5-Bromo-6-methylindoline-2,3-dione can be utilized as a key intermediate for the synthesis of pharmaceuticals, agrochemicals, and functional materials. Its ability to undergo diverse chemical transformations such as substitution, addition, and oxidation reactions makes it a valuable tool for organic chemists seeking to design and produce new compounds with specific properties. Additionally, the bromine atom in the molecule can serve as a directing group in various synthetic strategies, enabling selective functionalization at specific positions within a molecule. As a result, 5-Bromo-6-methylindoline-2,3-dione plays a crucial role in the development of advanced synthetic methodologies and the creation of novel molecules with potential applications in various industries.