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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, 1,1,3-trimethyl-

CC1=CC(c2c1cccc2)(C)C Request for Quotation
Chemical Name: 1H-Indene, 1,1,3-trimethyl-
CAS Number: 2177-45-9
Product Number: AG006ZEU(AGN-PC-0JTDMK)
Synonyms:
MDL No:
Molecular Formula: C12H14
Molecular Weight: 158.2396

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,1,3-Trimethyl-1H-indene is a versatile compound frequently utilized in chemical synthesis due to its unique structure and reactivity. When employed in organic reactions, this chemical serves as a valuable building block for the construction of various complex molecules. Its branched structure and substituted methyl groups allow for selective functionalization, enabling chemists to tailor the properties of the final products. In addition, the presence of a fused benzene ring in 1,1,3-Trimethyl-1H-indene provides aromatic characteristics that can impart specific properties to the synthesized compounds. Overall, its application in chemical synthesis offers a wide range of possibilities for creating novel structures and developing advanced materials.