2-Pentenoic acid, 5-(2-((4-bromophenyl)methoxy)cyclohexyl)-, methyl ester, (1alpha(Z),2beta)-

Base Information

Chemical Name:2-Pentenoic acid, 5-(2-((4-bromophenyl)methoxy)cyclohexyl)-, methyl ester, (1alpha(Z),2beta)-
CAS No.:101859-47-6
Molecular Formula:C₁₉H₂₅BrO₃
Molecular Weight:381.31
Hs Code.:

Synonyms:2-Pentenoic acid, 5-(2-((4-bromophenyl)methoxy)cyclohexyl)-, methyl ester, (1alpha(Z),2beta)-;101859-47-6

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

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Chemical Property of 2-Pentenoic acid, 5-(2-((4-bromophenyl)methoxy)cyclohexyl)-, methyl ester, (1alpha(Z),2beta)-

Chemical Property:

Vapor Pressure:3.54E-08mmHg at 25°C
Boiling Point:446.8°Cat760mmHg
Flash Point:224°C
Density:1.26g/cm³
XLogP3:4.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:8
Exact Mass:380.09871
Heavy Atom Count:23
Complexity:375

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC(=O)C=CCCC1CCCCC1OCC2=CC=C(C=C2)Br
Isomeric SMILES:COC(=O)/C=C\CC[C@H]1CCCC[C@@H]1OCC2=CC=C(C=C2)Br

Technology Process of 2-Pentenoic acid, 5-(2-((4-bromophenyl)methoxy)cyclohexyl)-, methyl ester, (1alpha(Z),2beta)-

There total 4 articles about 2-Pentenoic acid, 5-(2-((4-bromophenyl)methoxy)cyclohexyl)-, methyl ester, (1alpha(Z),2beta)- 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:

: 286-20-4
cyclohexane-1,2-epoxide

: 101859-47-6,101976-96-9
(E)-5-[(1R,2S)-2-(4-Bromo-benzyloxy)-cyclohexyl]-pent-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) CuI / 1.) Et₂O

2: KN(Me₄Si)2 / tetrahydrofuran; dimethylformamide

3: 1.) O₃, 2.) (CH₃)2S / 1.) MeOH, - 60 deg C

4: CHCl₃ / Heating

With copper(l) iodide; dimethylsulfide; KN(Me₄Si)2; ozone; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jo00362a014

Reference yield:

: 1773-36-0,3392-93-6,90974-59-7
trans-2-but-3-enylcyclohexanol

: 101859-47-6,101976-96-9
(E)-5-[(1R,2S)-2-(4-Bromo-benzyloxy)-cyclohexyl]-pent-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: KN(Me₄Si)2 / tetrahydrofuran; dimethylformamide

2: 1.) O₃, 2.) (CH₃)2S / 1.) MeOH, - 60 deg C

3: CHCl₃ / Heating

With dimethylsulfide; KN(Me₄Si)2; ozone; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jo00362a014

Reference yield:

: 101859-45-4
1-Bromo-4-((1S,2R)-2-but-3-enyl-cyclohexyloxymethyl)-benzene

: 101859-47-6,101976-96-9
(E)-5-[(1R,2S)-2-(4-Bromo-benzyloxy)-cyclohexyl]-pent-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) O₃, 2.) (CH₃)2S / 1.) MeOH, - 60 deg C

2: CHCl₃ / Heating

With dimethylsulfide; ozone; In chloroform;
DOI:10.1021/jo00362a014