2-Cyclopropene-1-carboxylic acid, 2-methyl-3-(4-chlorophenyl)-, methyl ester

Base Information

• Chemical Name: 2-Cyclopropene-1-carboxylic acid, 2-methyl-3-(4-chlorophenyl)-, methyl ester
• CAS No.: 69645-14-3
• Molecular Formula: C12H11ClO2
• Molecular Weight: 222.6675
• DSSTox Substance ID: DTXSID70989757
• Mol file: 69645-14-3.mol

Synonyms:2-Cyclopropene-1-carboxylic acid, 2-methyl-3-(4-chlorophenyl)-, methyl ester;69645-14-3;methyl 2-(4-chlorophenyl)-3-methylcycloprop-2-ene-1-carboxylate;DTXSID70989757

Chemical Property of 2-Cyclopropene-1-carboxylic acid, 2-methyl-3-(4-chlorophenyl)-, methyl ester

Chemical Property:

• Vapor Pressure: 0.00342mmHg at 25°C
• Boiling Point: 282.1°Cat760mmHg
• Flash Point: 132.4°C
• PSA: 26.30000
• Density: 1.263g/cm³
• LogP: 2.91630
• XLogP3: 2.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 222.0447573
• Heavy Atom Count: 15
• Complexity: 301

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(C1C(=O)OC)C2=CC=C(C=C2)Cl

Technology Process of 2-Cyclopropene-1-carboxylic acid, 2-methyl-3-(4-chlorophenyl)-, methyl ester

There total 3 articles about 2-Cyclopropene-1-carboxylic acid, 2-methyl-3-(4-chlorophenyl)-, methyl ester 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:

4-chloro-1-propynylbenzene (2809-65-6) + methyl diazoacetate (6832-16-2) → 2-p-Chlorphenyl-3-methyl-2-cyclopropen-1-carbonsaeuremethylester (69645-14-3)

Guidance literature:

With dirhodium tetraacetate;

Reference yield:

4-chloro-1-propynylbenzene (2809-65-6) → 2-p-Chlorphenyl-3-methyl-2-cyclopropen-1-carbonsaeuremethylester (69645-14-3)

Guidance literature:

Multi-step reaction with 2 steps

1: (i) Rh₂(OAc)4, (ii) NaOH

Reference yield:

diazomethane (186581-53-3,908094-01-9,334-88-3) + 2-p-Chlorphenyl-3-methyl-2-cyclopropen-1-carbonsaeure (18826-55-6) → 2-p-Chlorphenyl-3-methyl-2-cyclopropen-1-carbonsaeuremethylester (69645-14-3)

Guidance literature:

upstream raw materials:

diazomethane

2-p-Chlorphenyl-3-methyl-2-cyclopropen-1-carbonsaeure

4-chloro-1-propynylbenzene

methyl diazoacetate

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