Cyclopentanecarbonyl chloride

Base Information

• Chemical Name: Cyclopentanecarbonyl chloride
• CAS No.: 4524-93-0
• Molecular Formula: C6H9ClO
• Molecular Weight: 132.59
• Hs Code.: 29162000
• European Community (EC) Number: 224-856-1
• UNII: HZV3Z32TX8
• DSSTox Substance ID: DTXSID10196448
• Nikkaji Number: J205.893F
• Wikidata: Q72460291
• Mol file: 4524-93-0.mol

Synonyms:Cyclopentanecarbonyl chloride;4524-93-0;Cyclopentanecarbonylchloride;HZV3Z32TX8;Cyclopentane carboxyl chloride;CYCLOPENTANECARBOXYLIC ACID CHLORIDE;1-cyclopentanecarbonyl chloride;EINECS 224-856-1;MFCD00001370;Cyclopentanecarbonyl Chloride 98%;Cyclopentanoyl chloride;cyclopentylformyl chloride;Cyclopetanecarbonylchloride;cyclopentancarbonyl chloride;Cyclopentylcarbonyl chloride;UNII-HZV3Z32TX8;cyclopentane carbonylchloride;cyclopentyl carbonyl chloride;cyclopentan-ecarbonyl chloride;Cyclopentane carbonyl chloride;SCHEMBL101983;DTXSID10196448;Cyclopentanecarbonyl chloride, 98%;cyclopentane carboxylic acid chloride;BBL100048;STL511023;AKOS005256983;BP-11354;PS-10939;A7126;C2391;FT-0624261;D89509;EN300-133628;W-106158

Chemical Property of Cyclopentanecarbonyl chloride

Chemical Property:

• Appearance/Colour: clear colorless to yellow liquid
• Vapor Pressure: 2.27mmHg at 25°C
• Refractive Index: n20/D 1.4622(lit.)
• Boiling Point: 161.499 °C at 760 mmHg
• Flash Point: 62.466 °C
• PSA: 17.07000
• Density: 1.155 g/cm³
• LogP: 1.94200
• Sensitive.: Moisture Sensitive
• Water Solubility.: Reacts with water.
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 132.0341926
• Heavy Atom Count: 8
• Complexity: 94.7

Purity/Quality:

99% ^*data from raw suppliers

Cyclopentanecarbonyl chloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): C
• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-36/37/39-45

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1CCC(C1)C(=O)Cl
• Uses: Cyclopentanecarbonyl chloride is used in biochemical for proteomics research.

Technology Process of Cyclopentanecarbonyl chloride

There total 9 articles about Cyclopentanecarbonyl chloride 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: 100.0%

→ Cyclopentanecarboxylic acid chloride (4524-93-0)

Guidance literature:

Reference yield: 97.4%

cyclopentanecarboxylic acid (3400-45-1) → Cyclopentanecarboxylic acid chloride (4524-93-0)

Guidance literature:

With thionyl chloride; at 40 - 50 ℃; for 2h;

Reference yield: 86.4%

pyrrolidine (123-75-1) + chloro(chlorosulfanyl)methanone (2757-23-5) → Cyclopentanecarboxylic acid chloride (4524-93-0)

Guidance literature:

pyrrolidine; chloro(chlorosulfanyl)methanone; In dichloromethane; at 40 ℃; Inert atmosphere;

With chlorine; In dichloromethane; at 20 ℃;

DOI:10.1139/V10-138

upstream raw materials:

oxalyl dichloride

Cyclopentane

cyclopentanecarboxylic acid

cyclopent-1-enecarboxylic acid

Downstream raw materials:

(4-ethoxy-phenyl)-cyclopentyl ketone

phenyl cyclopentanecarboxylate

Cyclopentancarbonsaeure-2'-chlor-4',6'-dinitrophenylester

Cyclopentancarbonsaeure-2'-methyl-4',6'-dinitrophenylester

Refernces

• 1、 -. "THERAPEUTIC COMPOUNDS". Paragraph 00559-00561. . Retrieved 2021/06/04.
• 2、 -. "Lappaconitine derivative with analgesic activity, and preparation method and application thereof". Paragraph 0275-0279. . Retrieved 2021/07/14.