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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-Indene, 5-bromo-2,3-dihydro-1-methylene-

Brc1ccc2c(c1)CCC2=C Request for Quotation
Chemical Name: 1H-Indene, 5-bromo-2,3-dihydro-1-methylene-
CAS Number: 875306-81-3
Product Number: AG01EDZ0(AGN-PC-0CLW0L)
Synonyms:
MDL No:
Molecular Formula: C10H9Br
Molecular Weight: 209.0825

Identification/Properties

Computed Properties
Molecular Weight:
209.086g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
0
Exact Mass:
207.989g/mol
Monoisotopic Mass:
207.989g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
174
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


5-Bromo-2,3-dihydro-1-methylene-1H-indene is a versatile chemical compound that finds applications in various areas of chemical synthesis. This compound is commonly employed as a building block in the preparation of various organic molecules due to its unique structure and reactivity. In organic synthesis, 5-Bromo-2,3-dihydro-1-methylene-1H-indene serves as a valuable starting material for the synthesis of complex molecules with desired properties. Its reactivity allows for the introduction of different functional groups, leading to the formation of diverse chemical structures. Additionally, this compound can participate in various types of chemical reactions, such as substitution, addition, and cyclization reactions, making it a useful tool for chemists in designing and synthesizing new compounds with potential applications in pharmaceuticals, materials science, and agrochemicals. By utilizing 5-Bromo-2,3-dihydro-1-methylene-1H-indene in chemical synthesis, researchers can access a wide range of structural motifs and tailor-made molecules for specific applications in the field of chemistry.