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1-Propanone, 1-(4-chlorophenyl)-3-(1-piperidinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32594-52-8

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32594-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32594-52-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,5,9 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 32594-52:
(7*3)+(6*2)+(5*5)+(4*9)+(3*4)+(2*5)+(1*2)=118
118 % 10 = 8
So 32594-52-8 is a valid CAS Registry Number.

32594-52-8Relevant academic research and scientific papers

Evaluation of Cytotoxic Properties of N,N'-bis[(1-aryl-3-heteroaryl)propylidene]-hydrazine dihydrochlorides

Kucukoglu,Gul,Sakagami

, p. 784 - 787 (2020/11/23)

N,N'-bis[(1-aryl-3-heteroaryl)propylidene]hydrazine dihydrochlorides, P1, P4 – P8, and R1 – R7, were assayed against human oral squamous cell carcinoma (HSC-2, HSC-3, HSC-4), human promyelocytic leukemia cell line (HL-60), and human normal oral cells (HGF

Anticonvulsant activity of semicarbazone derivatives of Mannich bases

Pandeya,Sowmyalakshmi,Panda,Pandeya,Stables

, p. 2657 - 2661 (2007/10/03)

A series of semicarbazones of semicarbazide/p-chlorophenyl semicarbazide and Mannich bases of acetophenone/p-chloroacetophenone has been synthesized and their anticonvulsant activity screened against MES and scPTZ test. p-Chlorophenyl semi-carbazone of N,N-dimethylaminopropiophenone has been found to be the most active in all these tests.

Hypolipidemic activity of 3-amino-1-(2,3,4-mononitro-, mono-, or dihalophenyl) propan-1-ones in rodents

Huang, Yunsheng,Hall, Iris H.

, p. 339 - 346 (2007/10/03)

A series of 3-amino-1-(2,3,4-mononitro-, mono-, or dihalophenyl) propan-1-ones were synthesized and shown to be effective in lowering both serum cholesterol and triglyceride levels significantly in CF1 mice and Sprague-Dawley rats. All analogs

EFFECT OF THE STRUCTURE OF THE REAGENTS ON THE FORMATION RATE OF ARYL VINYL KETONES IN THE REACTION OF AMINES WITH β-HALOGENOPROPIOPHENONES

Popov, A. F.,Piskunova, Zh. P.,Matvienko, V. N.

, p. 1918 - 1921 (2007/10/02)

The dependence of the formation rate of aryl vinyl ketones in the reaction of ring-substituted β-halogenopropiophenones with various amines on the structure of the reagents was investigated.By analysis of the obtained data it was concluded that the process takes place by an E2 mechanism through an anion-like transition state.

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