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1-Piperidino-butane-2,3-dione-2-phenylhydrazone is a chemical compound with the molecular formula C16H22N2O2. It is a derivative of piperidine, a heterocyclic amine, and butane-2,3-dione, a diketone. The compound is characterized by the presence of a phenylhydrazone group, which is formed by the reaction of the diketone with phenylhydrazine. This results in the formation of a hydrazone linkage, which is a key structural feature of the compound. The compound is of interest in organic chemistry and may have potential applications in the synthesis of various pharmaceuticals and other chemical products due to its unique structure and reactivity.

733-18-6

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733-18-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 733-18-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 733-18:
(5*7)+(4*3)+(3*3)+(2*1)+(1*8)=66
66 % 10 = 6
So 733-18-6 is a valid CAS Registry Number.

733-18-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-piperidino-butane-2,3-dione-2-phenylhydrazone

1.2 Other means of identification

Product number -
Other names 1-Piperidino-2-phenylhydrazono-3-oxobutan

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 -
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More Details:733-18-6 SDS

733-18-6Relevant academic research and scientific papers

Studies on enamines and azaenamines: 2-Oxoarylhydrazonals as C-1 nucleophiles

Al-Mousawi, Saleh M.,Moustafa, Moustafa Sherief,Elnagdi, Mohamed Hilmy

experimental part, p. 2201 - 2211 (2011/04/16)

2-Oxoarylhydrazonals 1a,b react with aldehydes; piperidine; morpholine and benzotriazole to yield the corresponding Mannich bases 2a,f, and 4. Formaldehyde reacts with 1a,b to yield the hydroxymethylarylhyrazons 5a,b together with bisarylhydrazones 6. The hydroxymethyl derivatives 5a are converted to arylhydrazonal 7 upon oxidation in refluxing nitrobenzene. The reaction of aldehydes and malononitrile with 1a,b in ethanolic solution in presence of chitozan as heterogeneous catalyst afforded 6-amino-1,4-dihydropyridazins 14a,b. The Japan Institute of Heterocyclic Chemistry.

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