Chlorocyclopentane

Base Information

• Chemical Name: Chlorocyclopentane
• CAS No.: 930-28-9
• Molecular Formula: C5H9Cl
• Molecular Weight: 104.579
• Hs Code.: 29035990
• European Community (EC) Number: 213-212-5
• NSC Number: 16930
• UNII: TO3F41CL9A
• DSSTox Substance ID: DTXSID7061306
• Nikkaji Number: J100.777G
• Wikidata: Q2964117
• Mol file: 930-28-9.mol

Synonyms:Chlorocyclopentane;Cyclopentyl chloride;930-28-9;Cyclopentane, chloro-;chloro-cyclopentane;UNII-TO3F41CL9A;TO3F41CL9A;Chloroclopentane;EINECS 213-212-5;NSC-16930;AI3-23449;EC 213-212-5;Cyclopentylchloride;NSC16930;2-chlorocyclopentane;Chlorocyclopentane, 99%;SCHEMBL22512;DTXSID7061306;AMY22306;MFCD00001360;NSC 16930;AKOS009158983;PS-11986;FT-0623636;EN300-1262786;Q-200905;Q2964117

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Chemical Property of Chlorocyclopentane

Chemical Property:

• Appearance/Colour: clear colorless liquid
• Vapor Pressure: 24mmHg at 25°C
• Melting Point: -50 °C
• Refractive Index: n20/D 1.4512(lit.)
• Boiling Point: 114 °C at 760 mmHg
• Flash Point: 15 °C
• PSA: 0.00000
• Density: 1 g/cm³
• LogP: 2.16780
• Storage Temp.: Flammables area
• Solubility.: 0.8g/l
• Water Solubility.: 760 mg/L
• XLogP3: 2.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 104.0392780
• Heavy Atom Count: 6
• Complexity: 37.2

Purity/Quality:

Safty Information:

• Pictogram(s): F, Xi
• Hazard Codes: F,Xi
• Statements: 11-38
• Safety Statements: 16-9-37-33

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1CCC(C1)Cl
• Uses: Chlorocyclopentane was used in the preparation of diastereomeric activation products. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

Technology Process of Chlorocyclopentane

There total 23 articles about Chlorocyclopentane 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: 96.0%

Cyclopentane (287-92-3) → cyclopentyl chloride (930-28-9)

Guidance literature:

With potassium chloride; tetrabutyl-ammonium chloride; acetic acid; In water; at 20 ℃; for 6.5h; Reagent/catalyst;

Reference yield: 80.0%

Cyclopentanol (96-41-3) → cyclopentyl chloride (930-28-9) + cyclopentene (142-29-0)

Guidance literature:

With 1-chloro-1-(dimethylamino)-2-methyl-1-propene; In dichloromethane; 1.) 0 deg C; 2.) rt., 3h;

DOI:10.1016/S0040-4039(00)99407-3

Reference yield: 80.0%

cyclopentene (142-29-0) → Cyclopentanol (96-41-3) + cyclopentyl chloride (930-28-9)

Guidance literature:

With tetrachloromethane; copper(II) choride dihydrate; chromium(III) acetylacetonate; water; at 130 ℃; for 12h; Sealed tube;

DOI:10.1134/S1070428013100047

upstream raw materials:

Cyclopentane

Cyclopentanol

cyclopentyl chloroformate

trifluoroborane diethyl ether

Downstream raw materials:

2-cyclopentyl-2-phenyl-propionitrile

cyclopentyl methyl ether

cyclopentene

cyclopentyl-triphenyl-silane

Refernces

• 1、 Stockton,Lochte. "-". . p. 160. Retrieved 1945.
• 2、 Li, Zi-Hao,Fiser, Béla,Jiang, Biao-Lin,Li, Jian-Wei,Xu, Bao-Hua,Zhang, Suo-Jiang. "N -Hydroxyphthalimide/benzoquinone-catalyzed chlorination of hydrocarbon C-H bond using N -chlorosuccinimide". supporting information. p. 3403 - 3408. Retrieved 2019/04/01.
• 3、 -. "A alkane halogenation method (by machine translation)". Paragraph 0040; 0041; 0042; 0043; 0050-0053. . Retrieved 2017/07/21.