1122-99-2

Basic information

• Product Name: CYCLOPENTYLACETYL CHLORIDE
• Synonyms: CYCLOPENTYLACETYL CHLORIDE;Cyclopentaneacetyl chloride;2-cyclopentylethanoyl chloride
• CAS NO: 1122-99-2
• Molecular Formula: C₇H₁₁ClO
• Molecular Weight: 146.61
• Mol File: 1122-99-2.mol
• Article Data: 29

Chemical Properties

• Boiling Point: 57-58°C 10mm
• Flash Point: 57-58°C/10mm
• Appearance: /
• Density: 1.087
• Vapor Pressure: 0.678mmHg at 25°C
• Refractive Index: 1.4622
• Water Solubility: Reacts with water.
• Sensitive: Moisture Sensitive
• BRN: 1906113
• CAS DataBase Reference: CYCLOPENTYLACETYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: CYCLOPENTYLACETYL CHLORIDE(1122-99-2)
• EPA Substance Registry System: CYCLOPENTYLACETYL CHLORIDE(1122-99-2)

Safety Data

• Hazard Codes: Xn
• Statements: 34-52-36-22
• Safety Statements: 26-36/37/39
• RIDADR: 3265
• HazardClass: 8
• PackingGroup: II
• Hazardous Substances Data: 1122-99-2(Hazardous Substances Data)

Usage

Uses

Cyclopentylacetyl chloride is used as a pharmaceutical intermediate and in chemical research.

InChI:InChI=1/C7H11ClO/c8-7(9)5-6-3-1-2-4-6/h6H,1-5H2

Upstream product

• 1123-00-8 2-cyclopentylacetic acid 
• 5660-81-1 2-cyclopentylpropanedioic acid 

Downstream Products

• 18322-54-8 ethyl cyclopentylacetate 
• 68104-99-4 ethyl 4-cyclopentyl-3-oxobutanoate 
• 24188-99-6 2-cyclopentyl-1-(4-methoxyphenyl)ethan-1-one 
• 164472-98-4 benzyl-2-cyclopentyl acetate 
• 92645-50-6 [2-Chloro-4-(2-cyclopentyl-acetyl)-phenoxy]-acetic acid 
• 67656-51-3 Cyclopentyl-acetic acid 3-(2-bromo-acetyl)-5-(2-cyclopentyl-acetoxy)-phenyl ester 
• 41715-81-5 2'-cyclopentyl-2,3-dimethyl-4-methoxyacetophenone 
• 80520-91-8 Toluene-4-sulfonic acid 3-cyclopentyl-2-oxo-propyl ester 
• 923556-03-0 2-cyclopentyl-N-(4-fluorophenyl)acetamide 
• 1262632-76-7 methyl 3-(4-(5-(1,2-dithiolan-3-yl)pentanamido)phenyl)-2-(2-cyclopentylacetamido)propanoate 
• 1262632-81-4 3-(4-(5-(1,2-dithiolan-3-yl)pentanamido)phenyl)-2-(2-cyclopentylacetamido)-propanoic acid 
• 1262632-95-0 N-(4-(3-(butylamino)-2-(2-cyclopentylacetamido)-3-oxopropyl)phenyl)-5-(1,2-dithiolan-3-yl)pentanamide 
• 1262632-99-4 N-(4-(2-(2-cyclopentylacetamido)-3-((3,4-dimethoxyphenylethyl)amino)-3-oxopropyl)phenyl)-5-(1,2-dithiolan-3-yl)pentanamide 

Relevant articles and documents

Cell-specific calcineurin inhibition by a modified cyclosporin

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Metal complex, electroluminescent device containing metal complex and application of metal complex

The invention provides a metal complex, an electroluminescent device containing the metal complex and application of the electroluminescent device, the metal complex has an M(La)m(Lb)n structure, the metal complex provided by the invention can more effectively finely adjust the luminescence color and adjust the luminescence peak width, so that the half-peak width is narrowed, the luminescence color is more saturated, the device efficiency is improved, and the current efficiency and the external quantum efficiency are relatively high.

Remote Directed Isocyanation of Unactivated C(sp3)-H Bonds: Forging Seven-Membered Cyclic Ureas Enabled by Copper Catalysis

Reported herein is an unprecedented copper-catalyzed site-selective ?-C(sp3)-H bonds activation of aliphatic sulfonamides for constructing the synthetically useful seven-membered N-heterocycles. A key to success is the use of in-situ-formed amide radicals, to activate the inert C(sp3)-H bond, and inexpensive TMSNCO, as a coupling reagent under mild conditions. To the best of our knowledge, this represents the first use of alkylamine derivatives as a five-membered synthon to prepare a seven-membered N-heterocycles.