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1,1,3,3-Tetramethyl-2,3-dihydro-1H-indene

Base Information
  • Chemical Name:1,1,3,3-Tetramethyl-2,3-dihydro-1H-indene
  • CAS No.:4834-33-7
  • Molecular Formula:C13H18
  • Molecular Weight:174.286
  • Hs Code.:
  • European Community (EC) Number:958-873-7
  • DSSTox Substance ID:DTXSID10554564
  • Nikkaji Number:J1.231.263F
  • Wikidata:Q82435633
  • Mol file:4834-33-7.mol
1,1,3,3-Tetramethyl-2,3-dihydro-1H-indene

Synonyms:1,1,3,3-Tetramethyl-2,3-dihydro-1H-indene;4834-33-7;1,1,3,3-TETRAMETHYL-2H-INDENE;1,1,3,3-tetramethylindane;2,3-dihydro-1,1,3,3-tetramethyl-1h-indene;1,1,3,3 tetramethylindane;1,1,3,3-Tetramethyl-indan;DTXSID10554564;IWIWGFMIKABCFO-UHFFFAOYSA-N;AC6210;MFCD27995656;AKOS024263081;SY249429;EN300-113635;F8881-6095

Suppliers and Price of 1,1,3,3-Tetramethyl-2,3-dihydro-1H-indene
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 6 raw suppliers
Chemical Property of 1,1,3,3-Tetramethyl-2,3-dihydro-1H-indene
Chemical Property:
  • XLogP3:4.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:174.140850574
  • Heavy Atom Count:13
  • Complexity:178
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1(CC(C2=CC=CC=C21)(C)C)C
Technology Process of 1,1,3,3-Tetramethyl-2,3-dihydro-1H-indene

There total 1 articles about 1,1,3,3-Tetramethyl-2,3-dihydro-1H-indene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sulfuric acid; at 20 ℃; Product distribution; Mechanism; also deuterated olefins and reagent, var. time;
Guidance literature:
aluminium trichloride; In 1,2-dichloromethane; (2S)-N-methyl-1-phenylpropan-2-amine hydrate; hexane; toluene;
Guidance literature:
Multi-step reaction with 11 steps
1: aluminium trichloride / nitrobenzene
2: sulfuric acid; nitric acid
3: hydrogen / nickel / methanol
4: (i) NaNO2, aq. HCl, (ii) CuCl, aq. HCl
5: sulfuric acid; nitric acid
6: hydrogen / nickel / methanol
7: (i) aq. NaNO2, H2SO4, (ii) aq. H2SO4
8: potassium hydroxide / N,N-dimethyl-formamide
9: hydrogen; triethylamine / palladium on activated charcoal / methanol
10: (i) LiAlH4, Et2O, (ii) PBr3, Py, hexane, (iii) /BRN= 610776/, xylene
11: ethyloxirane
With ethyloxirane; potassium hydroxide; aluminium trichloride; sulfuric acid; hydrogen; nitric acid; triethylamine; palladium on activated charcoal; nickel; In methanol; nitrobenzene; N,N-dimethyl-formamide;
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