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Ethyl (4Z)-4-(phenylhydrazono)pentanoate is a chemical compound with the molecular formula C14H20N2O2. It is an organic ester derived from pentanoic acid, featuring a phenylhydrazone functional group. ethyl (4Z)-4-(phenylhydrazono)pentanoate is characterized by a double bond (Z-configuration) between the fourth and fifth carbon atoms of the pentanoic acid chain. The phenylhydrazone group is formed by the reaction of the carbonyl group of the pentanoic acid with phenylhydrazine, resulting in the formation of a hydrazone linkage. Ethyl (4Z)-4-(phenylhydrazono)pentanoate is a colorless to pale yellow liquid and is used in various chemical synthesis processes, particularly in the preparation of pharmaceuticals and other organic compounds. Its unique structure and properties make it a valuable intermediate in the synthesis of various biologically active molecules.

3397-38-4

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3397-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3397-38-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,9 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3397-38:
(6*3)+(5*3)+(4*9)+(3*7)+(2*3)+(1*8)=104
104 % 10 = 4
So 3397-38-4 is a valid CAS Registry Number.

3397-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (4Z)-4-(phenylhydrazinylidene)pentanoate

1.2 Other means of identification

Product number -
Other names Ethyl 4-Phenylhydrazonopentanoate

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:3397-38-4 SDS

3397-38-4Relevant academic research and scientific papers

Reaction of Lawesson's reagent with ester hydrazones: Synthesis of novel 3-thioxo-1,2,3-diazaphospholine derivatives

Chebil, Emna,Touil, Soufiane

experimental part, p. 297 - 302 (2011/12/04)

The reaction of ester hydrazones with Lawesson's reagent leads to a variety of new 3-thioxo-1,2,3-diazaphospholine derivatives. The reaction shows relative regioselectivity and gives in some cases a mixture of two diastereoisomers. The electronic and steric factors influencing the regioselectivity of the reaction are discussed.

The Application of Levulinic Acid and 5-Nitro-2-furylmethylene Diacetate in the Total Synthesis of Some Novel Biologically Active (5-Nitro-2-furyl)azomethines

Vlaovic, Djordje,Cetkovic, Gordana,Juranic, Ivan,Balaz, Jelica,Lajsic, Stevan,Djokovic, Dejan

, p. 931 - 939 (2007/10/02)

The syntheses and in vitro antibacterial and antifungal evaluation of certain (5-nitro-2-furyl)azomethines with different heterocyclic nuclei are described.

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