39098-75-4

Basic information

• Product Name: 3-Cyclohexylpropionyl chloride
• Synonyms: 3-CYCLOHEXYLPROPIONYL CHLORIDE;3-CYCLOHEXANEPROPIONYL CHLORIDE;3-CYCLOHEXANE PROPANOYL CHLORIDE;TIMTEC-BB SBB005478;cyclohexylpropionyl chloride;Cyclohexanepropanoyl chloride;3-CYCLOHEXYLPROPIONYL CHLORIDE 96%;Cyclohexanepropanoic acid chloride
• CAS NO: 39098-75-4
• Molecular Formula: C₉H₁₅ClO
• Molecular Weight: 174.67
• EINECS: 254-289-5
• Mol File: 39098-75-4.mol
• Article Data: 35

Chemical Properties

• Boiling Point: 124-126 °C (35 mmHg)
• Flash Point: 95.9 °C
• Appearance: clear slightly yellow liquid
• Density: 1.0345
• Vapor Pressure: 0.103mmHg at 25°C
• Refractive Index: 1.469-1.472
• CAS DataBase Reference: 3-Cyclohexylpropionyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Cyclohexylpropionyl chloride(39098-75-4)
• EPA Substance Registry System: 3-Cyclohexylpropionyl chloride(39098-75-4)

Safety Data

• Hazard Codes: C,Xn
• Statements: 34-51-36-22
• Safety Statements: 45-36/37/39-26
• Hazardous Substances Data: 39098-75-4(Hazardous Substances Data)

Usage

Chemical Properties

clear slightly yellow liquid

InChI:InChI=1/C9H15ClO/c1-7(9(10)11)8-5-3-2-4-6-8/h7-8H,2-6H2,1H3

Upstream product

• 695-12-5 vinylcyclohexane 
• 1124-63-6 3-cyclohexylpropan-1-ol 
• 501-52-0 3-Phenylpropionic acid 
• 701-97-3 cyclohexanepropionic acid 
• 41010-09-7 3-cyclohexylpropionitrile 
• 28239-43-2 Trichloro-1,1,1-cyclohexyl-3-propan 
• 4442-79-9 cyclohexylethan-1-ol 

Downstream Products

• 19740-01-3 3-cyclohexyl-1-(thiophen-2-yl)propan-1-one 
• 101778-57-8 3-cyclohexyl-propionic acid-[3-(2,5-dimethyl-pyrrol-1-yl)-propyl ester] 
• 942516-92-9 (Z)-4-(2-cyclohexylethylidene)-3-cyclohexylmethyl-oxetan-2-one 
• 126930-21-0 4-(Cyclohexylmethyl)acetessigsaeure-ethylester 
• 72299-19-5 3-Cyclohexyl-N,N-dipropyl-propionamide 
• 138404-89-4 3-Cyclohexyl-N-[3-(3-cyclohexyl-propionylamino)-2-hydroxy-propyl]-propionamide 
• 143668-91-1 (S)-prolinol amide of 3-cyclohexylpropionic acid 
• 223787-31-3 N-(2-benzoyl-4-chloro-phenyl)-3-cyclohexyl-propionamide 
• 651738-74-8 3-cyclohexyl-N-hydroxypropanamide 
• 65680-79-7 8-(β-cyclohexylpropionyloxy)-5-(1-hydroxy-2-ethylaminobutyl)carbostyril 
• 31480-67-8 3-cyclohexyl-1-(4-methoxyphenyl)propan-1-one 
• 72299-18-4 3-cyclohexyl-N,N-dimethylpropanamide 

Relevant articles and documents

Novel synthetic approach to alfaprostol key intermediates via Stille coupling with an alkyne

Novel intermediates based on the Corey skeleton for preparation of the ω-chain of non-halogenated unnatural prostaglandin analogues containing a triple bond at position 13–14 (PG numbering) were synthesized. The utilization of a novel synthetic approach towards a new tin intermediate, and subsequent Stille coupling opens up new possibilities for preparing these important pharmaceutical intermediates.

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.

CARBONIC ANHYDRASE INHIBITORS AND ANTIBIOTICS AGAINST MULTIDRUG RESISTANT BACTERIA

The invention described herein generally relates to novel therapeutic compounds, and in particular to carbonic anhydrase inhibitors as a narrow spectrum antibiotics against drug resistant bacteria and methods for treating those infection diseases in mammals using the described carbonic anhydrase inhibitors or a pharmaceutical formulation thereof.