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4-Chloro-1-phenyl-1H-pyrazol-3-ol is a chemical compound with the molecular formula C9H7ClN2O. It is a derivative of pyrazole, a heterocyclic compound consisting of a five-membered aromatic ring with two nitrogen atoms and one oxygen atom. The presence of a chlorine atom at the 4-position and a phenyl group at the 1-position gives 4-chloro-1-phenyl-1H-pyrazol-3-ol unique chemical properties. It is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its potential to form diverse molecular structures. The compound is typically synthesized through various chemical reactions, such as the condensation of phenylhydrazine with ethyl acetoacetate followed by chlorination. It is important to handle 4-chloro-1-phenyl-1H-pyrazol-3-ol with care, as it may have potential health risks and should be used in accordance with proper safety protocols.

7409-32-7

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7409-32-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7409-32-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7409-32:
(6*7)+(5*4)+(4*0)+(3*9)+(2*3)+(1*2)=97
97 % 10 = 7
So 7409-32-7 is a valid CAS Registry Number.

7409-32-7Downstream Products

7409-32-7Relevant academic research and scientific papers

One-pot regioselective synthesis of novel oximino ester-containing 1-aryl-4-chloro-3-oxypyrazoles as potential fungicides

Li, Yi,Liu, Yuan-Yuan,Chen, Nan-Qing,Lü, Kun-Zhi,Xiong, Xiao-Hui,Li, Jie

, p. 1269 - 1282 (2014)

A novel, functional-group-tolerant, and highly regioselective one-pot synthesis of six 4-chloro-1-aryl-3-oxypyrazoles, 8a-8f, containing an oximino ester moiety has been developed. Their structures were characterized by 1H- and 13C-N

Synthesis and fungicidal activity of novel chloro-containing 1-Aryl-3-oxypyrazoles with an oximino ester or oximino amide moiety

Liu, Yuanyuan,Li, Yi,Chen, Nanqing,Lv, Kunzhi,Zhou, Chao,Xiong, Xiaohui,Li, Fangshi

, p. 8140 - 8150 (2014/07/08)

Six novel chloro-containing 1-aryl-3-oxypyrazoles TMa-TMf with an oximino ester or an oximino amide moiety were prepared by the reaction of 1-aryl-1H-pyrazol-3-ols with benzyl bromide. Their structures were characterized by 1H-NMR, 13C-NMR, IR, MS, and elemental analysis. A preliminary in vitro bioassay indicated that compounds TMa, TMe and TMf displayed excellent fungicidal activity against Rhizoctonia solani and could be used as potential lead compounds for further development of novel fungicides.

A combined experimental and natural bonding orbital charges study on the one-pot regioselective synthesis of 4-chloropyrazoles

Li, Yi,Liu, Yuanyuan,Xu, Guanghui,Chen, Kai,He, Guangke,Huang, Bin

, p. 658 - 661 (2015/01/16)

The mechanism of a DMF-catalysed electrophilic/nucleophilic chlorination of pyrazole is illustrated with the aid of calculations of the natural bonding orbital charges. Its high regioselectivity and good functionality tolerance of nine pyrazole substrates

DMF-catalyzed direct and regioselective C-H functionalization: Electrophilic/nucleophilic 4-halogenation of 3-oxypyrazoles

Liu, Yuanyuan,He, Guangke,Chen, Kai,Jin, Yin,Li, Yufeng,Zhu, Hongjun

experimental part, p. 5323 - 5330 (2011/11/13)

A novel, straightforward, and highly regioselective 4-chlorination of 3-oxypyrazole derivatives in boiling thionyl chloride (SOCl2) in the presence of catalytic N,N-dimethylformamide (DMF) has been developed. This reaction likely proceeds through a DMF-catalyzed electrophilic/nucleophilic chlorination mechanism and involves electrophilic attack by SOCl2 and nucleophilic substitution by Cl- as the key steps. Based on this mechanism, the corresponding 4-bromination and 4-iodination of 3-oxypyrazoles have also been achieved in good yield by adding Br- and I -, respectively, to the reaction system. This halogenation method enables quick access to many original 4-halo-3-oxypyrazole series. A novel DMF-catalyzed electrophilic/nucleophilic 4-halogenation of 3-oxypyrazole derivatives has been developed. This halogenation procedure provides quick access to many novel 4-halo-3-oxypyrazole series.

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