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6-Oxanonanoic acid, also known as 6-oxohexanoic acid, is a colorless, crystalline organic compound with the chemical formula C6H10O3. It is a derivative of hexanoic acid, featuring a carbonyl group (C=O) at the sixth position of the carbon chain. This six-carbon dicarboxylic acid is an important intermediate in the synthesis of various chemicals, pharmaceuticals, and fragrances. 6-Oxanonanoic acid is soluble in water and has a melting point of 34-36°C. It is commonly used in the production of specialty polymers, agrochemicals, and as a building block for the synthesis of other complex organic molecules. Due to its reactivity, it is essential to handle 6-oxanonanoic acid with care, following proper safety protocols.

4144-58-5

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4144-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4144-58-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,4 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4144-58:
(6*4)+(5*1)+(4*4)+(3*4)+(2*5)+(1*8)=75
75 % 10 = 5
So 4144-58-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O3/c1-2-5-8(10)6-3-4-7-9(11)12/h2-7H2,1H3,(H,11,12)

4144-58-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-OXONONANOIC ACID

1.2 Other means of identification

Product number -
Other names n-butyrl n-valeric acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4144-58-5 SDS

4144-58-5Downstream Products

4144-58-5Relevant academic research and scientific papers

Azolium/Hydroquinone Organo-Radical Co-Catalysis: Aerobic C?C-Bond Cleavage in Ketones

Nakatsuji, Yuya,Kobayashi, Yusuke,Masuda, Sakyo,Takemoto, Yoshiji

supporting information, p. 2633 - 2637 (2021/02/03)

Organo-radical catalysts have recently attracted great interest, and the development of this field can be expected to broaden the applications of organocatalysis. Herein, the first example of a radical-generating system is reported that does not require any photoirradiation, radical initiators, or preactivated substrates. The oxidative C?C-bond cleavage of 2-substituted cyclohexanones was achieved using an azolium salt and a hydroquinone as co-catalysts. A catalytic mechanism was proposed based on the results of diffusion-ordered spectroscopy and cyclic voltammetry measurements, as well as computational studies.

Synthesis of biologically active substances based on phenoxyethanol derivatives

Kukovinets,Yamansarova,Kasradze,Lozhkina,Zainullin,Abdullin

, p. 673 - 677 (2007/10/03)

By reaction of phenoxyethanol with diverse structure acyl chlorides phenoxyethanol esters were synthesized containing in the molecule fragments of undecene acid and also of some ketocarboxylic acids. The latter acids were obtained by ozonation of alkylcyclenes. 2005 Pleiades Publishing, Inc.

Oxidation of 2-substituted cycloalkanones with cerium(IV) sulfate tetrahydrate in alcohols and acetic acid

He, Liangyou,Horiuchi, C. Akira

, p. 2515 - 2521 (2007/10/03)

The reaction of 2-substituted cycloalkanones with cerium(IV) sulfate tetrahydrate (CS) in alcohols and acetic acid gave the corresponding alkyl esters of oxo acids (80-96%) and oxo acids (78-96%), respectively, by oxidative cleavage of the C(R).C=O bond. In the case of 2-iodocycloalkanones in methanol, the dimethyl ester was obtained in good yield. A treatment of 5α-cholestan-3-one with CS in methanol produced 2-acetal 3-ester of 2,3-seco derivative in good yield. The effects of cerium(IV) and copper(II) salts are also discussed.

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