N-(2,3-Dihydro-1H-inden-4-yl)acetamide

Base Information

Chemical Name:N-(2,3-Dihydro-1H-inden-4-yl)acetamide
CAS No.:77802-37-0
Molecular Formula:C11H13NO
Molecular Weight:175.23
Hs Code.:
DSSTox Substance ID:DTXSID40506798
Wikidata:Q82362731

Synonyms:77802-37-0;N-Indan-4-ylacetamide;N-(2,3-Dihydro-1H-inden-4-yl)acetamide;4-acetylaminoindan;N-Indan-4-yl-acetamide;SCHEMBL1613763;DTXSID40506798;LVVKZNOWQZDHEA-UHFFFAOYSA-N;MFCD24549339;WS-00285

Suppliers and Price of N-(2,3-Dihydro-1H-inden-4-yl)acetamide

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
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price

Total 1 raw suppliers

Chemical Property of N-(2,3-Dihydro-1H-inden-4-yl)acetamide

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:175.099714038
Heavy Atom Count:13
Complexity:202

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=CC=CC2=C1CCC2

Technology Process of N-(2,3-Dihydro-1H-inden-4-yl)acetamide

There total 1 articles about N-(2,3-Dihydro-1H-inden-4-yl)acetamide 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:

: N-(5-(1-phenylvinyl)-2,3-dihydro-1H-inden-4-yl)acetamide

: 77802-37-0
N-(2,3-dihydro-1H-inden-4-yl)acetamide

: (S)-N-(5-(1-phenylethyl)-2,3-dihydro-1H-inden-4-yl)acetamide

: (R)-N-(5-(1-phenylethyl)-2,3-dihydro-1H-inden-4-yl)acetamide

Guidance literature:: With bis(1,5-cyclooctadiene)iridium(I) tetrafluoroborate; C₆₄H₈₀O₆P₂; hydrogen; In toluene; at 120 ℃; for 1h; Overall yield = 60 %; enantioselective reaction; Schlenk technique; Inert atmosphere; Sealed tube;
DOI:10.1021/jacs.8b04627

Reference yield: 100.0%

: 100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6
styrene

: 77802-37-0
N-(2,3-dihydro-1H-inden-4-yl)acetamide

: N-(5-(1-phenylethyl)-2,3-dihydro-1H-inden-4-yl)acetamide

Guidance literature:: With [Ir(1,5-cyclooctadiene)₂]triflate; 1,4-bis[bis(pentafluorophenyl)phosphino]butane; In 1,4-dioxane; at 120 ℃; for 48h; Inert atmosphere; Sealed tube;
DOI:10.1002/anie.201506581

Reference yield: 91.0%

: 394-46-7
2-fluorostyrene

: 77802-37-0
N-(2,3-dihydro-1H-inden-4-yl)acetamide

: (R)-N-(5-(1-(2-fluorophenyl)ethyl)-2,3-dihydro-1H-inden-4-yl)acetamide

Guidance literature:: With bis(1,5-cyclooctadiene)iridium(I) tetrafluoroborate; C₆₄H₈₀O₆P₂; In toluene; at 110 ℃; for 72h; enantioselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1021/jacs.8b04627