1H-Inden-1-one, 2-(acetyloxy)-2,3-dihydro-

Base Information

• Chemical Name: 1H-Inden-1-one, 2-(acetyloxy)-2,3-dihydro-
• CAS No.: 1579-15-3
• Molecular Formula: C11H10O3
• Molecular Weight: 190.199
• DSSTox Substance ID: DTXSID90342502
• Nikkaji Number: J276.184J
• Mol file: 1579-15-3.mol

Synonyms:1H-Inden-1-one, 2-(acetyloxy)-2,3-dihydro-;1579-15-3;2-acetoxy-1-indanone;1-Oxo-2-acetoxyindan;SCHEMBL943506;DTXSID90342502;1-Oxo-2,3-dihydro-1H-inden-2-yl acetate #

Chemical Property of 1H-Inden-1-one, 2-(acetyloxy)-2,3-dihydro-

Chemical Property:

• XLogP3: 1.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 190.062994177
• Heavy Atom Count: 14
• Complexity: 259

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)OC1CC2=CC=CC=C2C1=O

Technology Process of 1H-Inden-1-one, 2-(acetyloxy)-2,3-dihydro-

There total 3 articles about 1H-Inden-1-one, 2-(acetyloxy)-2,3-dihydro- 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:

Reference yield: 93.0%

C6H9MnO6 + 1H-inden-1-one (480-90-0) → 2-acetoxyindan-1-one (1579-15-3)

Guidance literature:

With water; In acetic acid; benzene; Heating;

DOI:10.1002/adsc.200606055

Reference yield: 40.0%

1H-inden-3-yl acetate (19455-83-5) → 2-acetoxyindan-1-one (1579-15-3) + indan-1,2-dione (16214-27-0) + 2-hydroxyindan-1-one (1579-16-4)

Guidance literature:

triphenylpyrylium tetrafluoroborate; In dichloromethane; for 1h; Irradiation; aq. K₂CrO₄ as filter;

DOI:10.1016/S0040-4020(01)96217-9

Reference yield: 31.0%

1H-inden-3-yl acetate (19455-83-5) → 2-acetoxyindan-1-one (1579-15-3) + 2-acetylindan-1-one (5350-68-5) + 2-hydroxyindan-1-one (1579-16-4) + anti-1,2-diacetoxydibenzo tricyclo<5.3.0.0 2,6> decane (138610-99-8)

Guidance literature:

In hexane; for 6h; Irradiation;

DOI:10.1016/S0040-4020(01)96217-9

upstream raw materials:

1H-inden-3-yl acetate

1H-inden-1-one

Downstream raw materials:

(4aS,9bR)-4-Cyclohexyl-2,3,4,4a,5,9b-hexahydro-indeno[1,2-b][1,4]oxazine

1H-inden-1-one

cis-1,2-indandiol

(4aS,9bR)-4-Benzyl-2,3,4,4a,5,9b-hexahydro-indeno[1,2-b][1,4]oxazine; hydrochloride