Ethyl (2-(4-(1,4-dioxaspiro(4.5)dec-6-ylmethyl)phenoxy)ethyl)carbamate

Base Information

Chemical Name:Ethyl (2-(4-(1,4-dioxaspiro(4.5)dec-6-ylmethyl)phenoxy)ethyl)carbamate
CAS No.:118025-42-6
Molecular Formula:C₂₀H₂₉NO₅
Molecular Weight:363.454
Hs Code.:
DSSTox Substance ID:DTXSID40922595
Nikkaji Number:J893.906C
ChEMBL ID:CHEMBL369221
Mol file:118025-42-6.mol

Synonyms:NIOSH/FA4355000;118025-42-6;FA43550000;Ethyl (2-(4-((1,4-dioxaspiro(4.5)dec-6-yl)methyl)phenoxy)ethyl)carbamate;Carbamic acid, (2-(4-((1,4-dioxaspiro(4.5)dec-6-yl)methyl)phenoxy)ethyl)-, ethyl ester;Ethyl (2-(4-(1,4-dioxaspiro(4.5)dec-6-ylmethyl)phenoxy)ethyl)carbamate;CHEMBL369221;DTXSID40922595;Carbamic acid, (2-(4-(1,4-dioxaspiro(4.5)dec-6-ylmethyl)phenoxy)ethyl)-, ethyl ester;Ethyl hydrogen (2-{4-[(1,4-dioxaspiro[4.5]decan-6-yl)methyl]phenoxy}ethyl)carbonimidate;ethyl N-[2-[4-[[2,2-(ethylenedioxy)cyclohexyl]methyl] phenoxy]ethyl]carbamate

Suppliers and Price of Ethyl (2-(4-(1,4-dioxaspiro(4.5)dec-6-ylmethyl)phenoxy)ethyl)carbamate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of Ethyl (2-(4-(1,4-dioxaspiro(4.5)dec-6-ylmethyl)phenoxy)ethyl)carbamate

Chemical Property:

Vapor Pressure:3.92E-11mmHg at 25°C
Boiling Point:525.4°Cat760mmHg
Flash Point:271.6°C
Density:1.16g/cm³
XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:363.20457303
Heavy Atom Count:26
Complexity:430

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)NCCOC1=CC=C(C=C1)CC2CCCCC23OCCO3

Technology Process of Ethyl (2-(4-(1,4-dioxaspiro(4.5)dec-6-ylmethyl)phenoxy)ethyl)carbamate

There total 6 articles about Ethyl (2-(4-(1,4-dioxaspiro(4.5)dec-6-ylmethyl)phenoxy)ethyl)carbamate 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: 23.0%

: 6329-26-6
ethyl N-(2-chloroethyl)carbamate

: 80826-41-1
2-(4-hydroxybenzyl)-1-cyclohexanone ethylene acetal

: 118025-42-6
ethyl N-{2-[4-(2,2-ethylenedioxy-1-cyclohexylmethyl)phenoxy]ethyl} carbamate

Guidance literature:

Reference yield:

: 22081-10-3
2-(4-Hydroxybenzyl)-1-cyclohexanone

: 118025-42-6
ethyl N-{2-[4-(2,2-ethylenedioxy-1-cyclohexylmethyl)phenoxy]ethyl} carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: 80 percent / NaOH / H₂O / 6 h / Heating

2: 88 percent / NH₃ / tetrahydrofuran / -78 deg C to room t.

3: 45percent NaOH / benzene; H₂O / Ambient temperature

4: benzene / 4 h / Heating

With sodium hydroxide; ammonia; In tetrahydrofuran; water; benzene;
DOI:10.1002/hlca.19940770218

Reference yield:

: 116026-78-9
2-<4-(2-bromoethoxy)benzyl>-1-cyclohexanone

: 118025-42-6
ethyl N-{2-[4-(2,2-ethylenedioxy-1-cyclohexylmethyl)phenoxy]ethyl} carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / NH₃ / tetrahydrofuran / -78 deg C to room t.

2: 45percent NaOH / benzene; H₂O / Ambient temperature

3: benzene / 4 h / Heating

With sodium hydroxide; ammonia; In tetrahydrofuran; water; benzene;
DOI:10.1002/hlca.19940770218