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Ethyl (2Z)-2-(hydroxyimino)pentanoate is an organic compound with the chemical formula C7H13NO3. It is a colorless liquid with a molecular weight of 159.18 g/mol. ethyl (2Z)-2-(hydroxyimino)pentanoate is a derivative of pentanoic acid, featuring a hydroxyimino group and an ethyl ester group. It is synthesized by reacting ethyl 2-oxopentanoate with hydroxylamine, and it is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound is characterized by its Z-configuration, indicating the presence of a double bond with a specific geometric arrangement of substituents. It is soluble in organic solvents and has a pungent odor. Ethyl (2Z)-2-(hydroxyimino)pentanoate is an important building block in the chemical industry due to its versatile reactivity and potential applications in the production of various compounds.

7463-34-5

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7463-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7463-34-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7463-34:
(6*7)+(5*4)+(4*6)+(3*3)+(2*3)+(1*4)=105
105 % 10 = 5
So 7463-34-5 is a valid CAS Registry Number.

7463-34-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-hydroxyiminopentanoate

1.2 Other means of identification

Product number -
Other names 2-hydroxyimino-valeric acid ethyl ester

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:7463-34-5 SDS

7463-34-5Relevant academic research and scientific papers

Titanium(IV) enolates of 2-nitrocarboxylic esters and their oxidative chlorinationa convenient route to α-chloro-α-nitrocarboxylates

Ciez, Dariusz,Kalinowska-T?us?cik, Justyna

supporting information; experimental part, p. 267 - 271 (2012/03/11)

A new method for the synthesis of 2-chloro-2-nitrocarboxylic esters from 2-nitrocarboxylates is described. The procedure consists of the oxidative chlorination of titanium(IV) enolates of 2-nitro esters in the presence of ammonium nitrate. Esters of 2-chloro-2-nitrocarboxylic acids are formed in very good to quantitative yields. Application of this method for the chlorination of α,α′-dinitrodicarboxylates leads to α,α′- dichloro-α,α′-dinitrocarboxylic esters with high meso-diastereoselectivity. The absence of ammonium nitrate from the reaction mixture affects the reduction of nitro groups and leads to partial transformation of 2-nitrocarboxylic esters into 2-(hydroxyimino)carboxylates. Georg Thieme Verlag Stuttgart - New York.

New Synthesis of α-Nitroso Esters and Oximes of α-Keto Esters

Ali, Syed Masarrat,Matsuda, Yoshihiko,Tanimoto, Shigeo

, p. 805 - 806 (2007/10/02)

Ketene O-alkyl O'-silyl acetals on reaction with nitric oxide or isoamyl nitrite in the presence of titanium(IV) chloride provide either one of α-nitroso esters and oximes of α-keto esters.

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