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Acetaldehyde, oxime, (E)-, also known as (E)-2-Methylpentanal oxime, is an organic compound with the chemical formula C6H13NO. It is a colorless liquid that is formed by the reaction of acetaldehyde with hydroxylamine. Acetaldehyde, oxime, (E)- is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a reagent in the detection of aldehydes and ketones. The (E)-isomer indicates that the oxime group is in the trans configuration relative to the methyl group. Acetaldehyde, oxime, (E)- is a versatile building block in organic chemistry, and its properties and reactivity make it a valuable component in the synthesis of a wide range of products.

5780-37-0

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5780-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5780-37-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,8 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5780-37:
(6*5)+(5*7)+(4*8)+(3*0)+(2*3)+(1*7)=110
110 % 10 = 0
So 5780-37-0 is a valid CAS Registry Number.

5780-37-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-acetaldoxime

1.2 Other means of identification

Product number -
Other names -

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:5780-37-0 SDS

5780-37-0Relevant academic research and scientific papers

Clean synthesis of acetaldehyde oxime through ammoximation on titanosilicate catalysts

Ding, Jianghong,Xu, Le,Yu, Yejun,Wu, Haihong,Huang, Shijie,Yang, Yulin,Wu, Jing,Wu, Peng

, p. 2587 - 2595 (2013)

Acetaldehyde oxime has been synthesized though the liquid-phase ammoximation of acetaldehyde with ammonia and hydrogen peroxide over various titanosilicate catalysts. Titanium mordenite (Ti-MOR), prepared from highly dealuminated mordenite and TiCl4 vapor by a secondary synthesis method, was superior to TS-1 and Ti-MWW catalysts both in aldehyde conversion and in oxime selectivity. The reaction parameters were investigated systematically in a batch-type reactor for Ti-MOR, such as solvent effect, temperature, time, catalyst loading, amounts of ammonia and hydrogen peroxide relative to aldehyde as well as addition methods of the reactants. Under optimized conditions, Ti-MOR was capable of showing an aldehyde conversion of 99% and an oxime selectivity of 97%. In comparison with TS-1 and Ti-MWW, the advantage of Ti-MOR in acetaldehyde ammoximation was mainly attributed to its lower ability for oxidation to convert the aldehyde to acetic acid. There was almost no effect resulting from the addition mode of the reactants; Ti-MOR with its special characteristics was unique in catalytic behavior and easy handling. An overview of the reaction routes involved in acetaldehyde ammoximation has been provided.

One-step C=N, C=O bonds cleavage and C=O, C=N bonds formation over supported ionic liquid in water

Li, Dongmei,Shi, Feng,Deng, Youquan

, p. 6791 - 6794 (2007/10/03)

At ambient reaction temperature, the silica gel confined ionic liquid catalysts were perfectly combined with water as an effective catalytic system for simultaneous C=N and C=O bonds transformation with a TONs exceeding 300 mol mol-1.

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