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1-Hexanone, 1-(5-chloro-2-hydroxyphenyl)-, also known as 5-Chloro-2-hydroxyphenyl hexan-1-one, is an organic compound with the molecular formula C12H17ClO2. It is a colorless to pale yellow liquid with a molecular weight of 226.7 g/mol. 1-Hexanone, 1-(5-chloro-2-hydroxyphenyl)- is characterized by the presence of a 5-chloro-2-hydroxyphenyl group attached to a hexanone moiety, which consists of a six-carbon aliphatic chain with a ketone functional group at the end. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its chemical structure, it may exhibit properties such as reactivity with nucleophiles and electrophiles, as well as potential applications in the formation of complex organic molecules.

3226-16-2

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3226-16-2 Usage

Appearance

White to light yellow crystalline powder

Melting point

138-140°C

Common uses

Building block in the synthesis of pharmaceutical and agricultural products

Properties

Antibacterial, antifungal, and antioxidant

Safety precautions

May cause irritation to skin, eyes, and respiratory system upon contact or inhalation

Check Digit Verification of cas no

The CAS Registry Mumber 3226-16-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,2 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3226-16:
(6*3)+(5*2)+(4*2)+(3*6)+(2*1)+(1*6)=62
62 % 10 = 2
So 3226-16-2 is a valid CAS Registry Number.

3226-16-2Relevant academic research and scientific papers

Asymmetric synthesis of 3-benzofuranones through 5-exo-trig cyclization of 4-nitroaryl olefins

Verma, Nishant,Kumar, Sumit,Ahmed, Naseem

supporting information, p. 3547 - 3550 (2016/07/18)

Organo-catalyzed aldol condensation of 2-hydroxyacetophenone and 4-nitrobenzaldehyde underwent regio- and enantioselective cyclization via intramolecular 5-exo-trigonal cyclization to give 4-nitroaryl-3-benzofuranones. The product formation indicated that

Piperidine-mediated annulation of 2-acylphenols with 4-nitrobenzaldehyde to 3-benzofuranones

Verma, Nishant,Kundi, Varun,Ahmed, Naseem

supporting information, p. 4175 - 4179 (2015/06/22)

Piperidine - mediated reactions of 2-acylphenols and 4-nitrobenzaldehydes afforded 3-benzofuranones in high yield (82-95%) at reflux temperature in ethanol. The electron density calculation of HOMO-LUMO energy in the chalcone intermediates by DFT showed t

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