2,3-Dihydro-1H-inden-1-ylacetonitrile

Base Information

Chemical Name:2,3-Dihydro-1H-inden-1-ylacetonitrile
CAS No.:26452-99-3
Molecular Formula:C11H11N
Molecular Weight:157.21200
Hs Code.:2926909090
DSSTox Substance ID:DTXSID50452914
Mol file:26452-99-3.mol

Synonyms:2,3-DIHYDRO-1H-INDEN-1-YLACETONITRILE;26452-99-3;2-(2,3-dihydro-1H-inden-1-yl)acetonitrile;SCHEMBL627090;DTXSID50452914;AKOS006302279;AB60218;EN300-1853174

Suppliers and Price of 2,3-Dihydro-1H-inden-1-ylacetonitrile

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 4 raw suppliers

Chemical Property of 2,3-Dihydro-1H-inden-1-ylacetonitrile

Chemical Property:

PSA：23.79000
LogP:2.63008
XLogP3:2.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:157.089149355
Heavy Atom Count:12
Complexity:200

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC2=CC=CC=C2C1CC#N

Technology Process of 2,3-Dihydro-1H-inden-1-ylacetonitrile

There total 15 articles about 2,3-Dihydro-1H-inden-1-ylacetonitrile 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: 89.0%

: 156963-20-1
N-(2,2a,7,7a-tetrahydro-1H-cyclobut<α>indene-1-ylidene)-benzenesulfenamide

: 26452-99-3
2,3-dihydro-1H-indene-1-acetonitrile

: 131251-86-0
cis-2,3-dihydro-1-methyl-1H-indene-2-carbonitrile

Guidance literature:: With tri-n-butyl-tin hydride; 2,2'-azobis(isobutyronitrile); In cyclohexane; for 4h; Heating;
DOI:10.1016/S0040-4020(01)80850-4

Reference yield: 89.0%

: 131251-80-4
C₁₇H₁₅NS

: 26452-99-3
2,3-dihydro-1H-indene-1-acetonitrile

: 131251-86-0
cis-2,3-dihydro-1-methyl-1H-indene-2-carbonitrile

Guidance literature:: With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In cyclohexane; Product distribution; Mechanism; Heating; other S-phenyl sulphenylimines derived from cyclobutanones; methyl acrylate;
DOI:10.1021/ja00003a057