Ethyl bicyclo[2.2.1]hept-2-ylacetate

Base Information

Chemical Name:Ethyl bicyclo[2.2.1]hept-2-ylacetate
CAS No.:35658-04-9
Molecular Formula:C11H18 O2
Molecular Weight:182.263
Hs Code.:2916209090
European Community (EC) Number:252-658-5
DSSTox Substance ID:DTXSID20957042
Nikkaji Number:J260.661E
Mol file:35658-04-9.mol

Synonyms:35658-04-9;ETHYL BICYCLO[2.2.1]HEPT-2-YLACETATE;ethyl 2-(bicyclo[2.2.1]heptan-2-yl)acetate;EINECS 252-658-5;Ethyl bicyclo(2.2.1)hept-2-ylacetate;ethyl 2-(2-bicyclo[2.2.1]heptanyl)acetate;ETHYL 2-{BICYCLO[2.2.1]HEPTAN-2-YL}ACETATE;SCHEMBL11603168;DTXSID20957042;AUTDAVPVPASYDM-UHFFFAOYSA-N;AKOS008947923;Ethyl (bicyclo[2.2.1]heptan-2-yl)acetate;CS-0236436;NS00058218;G29986;EN300-1709736

Suppliers and Price of Ethyl bicyclo[2.2.1]hept-2-ylacetate

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

American Custom Chemicals Corporation
ETHYL-BICYCLO[2.2.1]HEPT-2-YLACETATE 95.00%
5MG
$ 497.53

Total 5 raw suppliers

Chemical Property of Ethyl bicyclo[2.2.1]hept-2-ylacetate

Chemical Property:

Vapor Pressure:0.0524mmHg at 25°C
Boiling Point:234.6°Cat760mmHg
Flash Point:88.9°C
PSA：26.30000
Density:1.016g/cm³
LogP:2.37580
XLogP3:2.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:182.130679813
Heavy Atom Count:13
Complexity:200

Purity/Quality:

99% ^*data from raw suppliers

ETHYL-BICYCLO[2.2.1]HEPT-2-YLACETATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)CC1CC2CCC1C2

Technology Process of Ethyl bicyclo[2.2.1]hept-2-ylacetate

There total 7 articles about Ethyl bicyclo[2.2.1]hept-2-ylacetate 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: 55.0%

: 498-66-8
norborn-2-ene

: 4455-13-4
methylthioacetic acid ethyl ester

: 35658-04-9
norbornylacetic acid ethyl ester

Guidance literature:: In ethanol; at 18 - 20 ℃; for 2.5h;
DOI:10.1016/S0040-4039(97)10095-8

Reference yield:

: (C₇H₁₁)-CH-(COOC₂H₅)BCl₂

: 35658-04-9
norbornylacetic acid ethyl ester

Guidance literature:: With Na₂CO₃; In water;
DOI:10.1021/jo00954a044

Reference yield:

: 623-73-4
diazoacetic acid ethyl ester

: 498-66-8
norborn-2-ene

: (C₂H₅)2O*(chloro)dihydroborane

: 35658-04-9
norbornylacetic acid ethyl ester

Guidance literature:: synthesis of (di-exo-norbornyl)chloroborane from norbornene and chloroborane etherate, react. with diazoaceticester, followed by hydrolysis;
DOI:10.1021/ja00765a086