Product classification

Contact us

Tel：0086-21-56469616
Phone：0086-18019205509
Website：https://www.minstargroup.com
Email： minstar@minstargroup.com
Address：BUILDING 8, NO.1098, CHUANSHA ROAD, PUDONG, SHANGHAI, CHINA

764-85-2

Product Name:Nonanoyl chloride
Molecular Formula:C₉H₁₇ClO
Appearance:clear slightly yellow liquid

Inquiry

Product Details

Appearance:clear slightly yellow liquid

Purity:99%

Factory Supply Nonanoyl chloride 764-85-2, Fast Delivery

764-85-2 Name
Name	Nonanoyl chloride
Synonym	PELARGONIC ACID CHLORIDE;PELARGONOYL CHLORIDE;PELARGONYL CHLORIDE;N-NONANOYL CHLORIDE;NONYL ACID CHLORIDE;NONANOYL CHLORIDE;NNCL;Nonanoic acid chloride

764-85-2 Chemical & Physical Properties
Melting point	-60.5 °C
Boiling point	214.7±3.0 °C at 760 mmHg
Density	1.0±0.1 g/cm3
Molecular Formula	C9H17ClO
Molecular Weight	176.684
Flash Point	95.0±0.0 °C
PSA	17.07000
LogP	4.18
Exact Mass	176.096786
Vapour Pressure	0.2±0.4 mmHg at 25°C
Index of Refraction	1.437

Nonanoyl chloride 764-85-2 Usage

Nonanoyl chloride is clear slightly yellow liquid, which is used for the acylation of amine groups of chitosan to simultaneously improve its material properties and adsorption capacity. It was also used in the synthesis of N-nonanoyl piperonylamide, caged vanilloid, N-(4-hydroxy-3-methoxybenzyl)-N-(2-nitrobenzyl)-nonanoylamide or N-(2-Nitrobenzyl)-N-vanillyl-nonanoylamide, n-benzylnonanamide.

InChI:InChI=1/C9H17ClO/c1-2-3-4-5-6-7-8-9(10)11/h2-8H2,1H3

764-85-2 Relevant articles

Pseudotrienic acids A and B, two bioactive metabolites from Pseudomonas sp. MF381-IODS

Pohanka, Anton,Broberg, Anders,Johansson, Maria,Kenne, Lennart,Levenfors, Jolanta

, p. 1380 - 1385 (2005)

Bioassay-guided fractionation of the liquid culture broth of Pseudomonas sp. MF381-IODS yielded two new antimicrobial substances, identified as (2E,4E,6E)-9-[((2S,3R)-3-hydroxy-4-{(3E,5E,7RS)-7-hydroxy-4-methylhexadeca-3, 5-dienoyl]amino}-2-methylbutanoyl)amino]nona-2,4,6-trienoic acid and the tetradeca equivalent, named pseudotrienic acids A (1) and B (2), respectively. Two known antimicrobial compounds, the polyketide 2,3-deepoxy-2,3-didehydrorhizoxin (3) and the tryptophan-derived pyrrolnitrin (4), were also identified.

Anion receptors with nitrone C–H hydrogen bond donors

Xuxian He, Richard R. Thompson, Sarah A. Clawson, Frank R. Fronczek and Semin Lee

Chemical Communications, 2023

The following esterification using nonanoyl chloride in the presence of triethylamine gave the desire. We report the use of nitrone C–H groups as hydrogen bond donors for binding anions. Acyclic anion receptors with two nitrone moieties were synthesized by condensation reactions between aryl-aldehydes and m-phenylenedihydroxylamines.

764-85-2 Process route

: 112-05-0
nonanoic acid

: 764-85-2
Nonanoyl chloride

Conditions

Conditions	Yield
With thionyl chloride; for 4h; Reflux;	99%
With zinc(II) chloride; phosphorus trichloride;
With thionyl chloride;
With thionyl chloride;
With oxalyl dichloride;
With oxalyl dichloride; Ambient temperature;
With thionyl chloride; Heating;
With oxalyl dichloride; for 3h;
With thionyl chloride; In benzene; Heating;
With thionyl chloride; for 3h; Heating;
With oxalyl dichloride;
With thionyl chloride; In benzene; Heating;
With thionyl chloride; N,N-dimethyl-formamide; at 50 ℃; for 2.25h;
With phosgene; N,N-dimethyl-formamide; at 20 - 30 ℃;
With hydrogenchloride; phosgene; N,N-dimethyl-formamide; at 20 - 30 ℃;
With oxalyl dichloride; In dichloromethane; at 0 - 20 ℃; for 2h;
With thionyl chloride; In chloroform; at 65 ℃; for 0.5h;
With trichloroacetamide; triphenylphosphine; In dichloromethane; for 1h; Reflux;
With oxalyl dichloride;
With thionyl chloride;
With thionyl chloride; for 2h; Reflux; Cooling with ice;
With thionyl chloride; Reflux;
With thionyl chloride; at 80 ℃; for 16h;
With thionyl chloride; for 4h; Reflux;
With thionyl chloride; In N,N-dimethyl-formamide; at 70 ℃;
With oxalyl dichloride; In dichloromethane; at 20 ℃;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 20 ℃; for 2h;
With thionyl chloride; at 70 ℃; for 4h;
With oxalyl dichloride;
With oxalyl dichloride;
With oxalyl dichloride; In dichloromethane; at 20 ℃; for 0.166667h;
With trichloroacetamide; triphenylphosphine; In dichloromethane; for 1h; Reflux;
With oxalyl dichloride; In dichloromethane; at 0 - 20 ℃; for 2h; Inert atmosphere;
With thionyl chloride; Reflux;
With thionyl chloride; Reflux;
With thionyl chloride; In dichloromethane; N,N-dimethyl acetamide; at 0 - 10 ℃; for 0.5h;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 0 - 20 ℃; for 2h;