2-Naphthaleneacetonitrile, 5,6,7,8-tetrahydro-

Base Information

Chemical Name:2-Naphthaleneacetonitrile, 5,6,7,8-tetrahydro-
CAS No.:3160-18-7
Molecular Formula:C12H13N
Molecular Weight:171.23800
Hs Code.:
Mol file:3160-18-7.mol

Synonyms:(5,6,7,8-Tetrahydro-[2]naphthyl)-acetonitril;(5,6,7,8-tetrahydro-[2]naphthyl)-acetonitrile;1.2.3.4-Tetrahydronaphthyl-7-acetonitril;2-Cyanmethyl-5,6,7,8-tetrahydro-naphthalin;5,6,7,8-tetrahydronaphthalene-2-acetonitrile;

Suppliers and Price of 2-Naphthaleneacetonitrile, 5,6,7,8-tetrahydro-

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

Labseeker
2-NAPHTHALENEACETONITRILE,5,6,7,8-TETRAHYDRO 95
10g
$ 3208.00

Total 5 raw suppliers

Chemical Property of 2-Naphthaleneacetonitrile, 5,6,7,8-tetrahydro-

Chemical Property:

PSA：23.79000
LogP:2.63148

Purity/Quality:

99% ^*data from raw suppliers

2-NAPHTHALENEACETONITRILE,5,6,7,8-TETRAHYDRO 95 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2-Naphthaleneacetonitrile, 5,6,7,8-tetrahydro-

There total 5 articles about 2-Naphthaleneacetonitrile, 5,6,7,8-tetrahydro- 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:

: 3160-18-7
<6-(1,2,3,4-tetrahydronaphthalenyl)>acetonitrile

Guidance literature:: With thionyl chloride; benzene;
DOI:10.1021/ja01174a003

Reference yield:

: 119-64-2
tetralin

: 3160-18-7
<6-(1,2,3,4-tetrahydronaphthalenyl)>acetonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: conc. aq. HCl, HCl(gas) / benzene / 1.5 h / Ambient temperature

2: dimethylsulfoxide / 18 h / Ambient temperature

With hydrogenchloride; In dimethyl sulfoxide; benzene;
DOI:10.1021/jm00085a002

Reference yield:

: 6883-81-4
6-hydroxymethyl-1,2,3,4-tetrahydronaphthalene

: 3160-18-7
<6-(1,2,3,4-tetrahydronaphthalenyl)>acetonitrile

Guidance literature:: With thionyl chloride; benzene; Erhitzen des Reaktionsprodukts mit Natriumcyanid in wss. Methanol;
DOI:10.1021/ja01246a027