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2671-84-3

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2671-84-3 Usage

General Description

Ethanone, 1-(4-ethoxyphenyl)-, oxime, also known as ethoxyphenyl ketoxime, is a compound with the chemical formula C10H13NO2. It is used as a reagent in organic synthesis for the transformation of ketones to oximes. Oximes are important intermediates in the preparation of various functionalized organic compounds and can also be used as ligands in coordination chemistry. Ethanone, 1-(4-ethoxyphenyl)-, oxime is a colorless to pale yellow solid with a melting point of around 81-84 degrees Celsius. It possesses a sweet floral odor and is sparingly soluble in water but soluble in organic solvents.

Check Digit Verification of cas no

The CAS Registry Mumber 2671-84-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,7 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2671-84:
(6*2)+(5*6)+(4*7)+(3*1)+(2*8)+(1*4)=93
93 % 10 = 3
So 2671-84-3 is a valid CAS Registry Number.

2671-84-3SDS

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 1-(4-ethoxy-phenyl)-ethanone oxime

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:2671-84-3 SDS

2671-84-3Relevant articles and documents

Facile preparation of 5-alkyl-1-aryltetrazoles with arenes, acyl chlorides, hydroxylamine, and diphenylphosphoryl azide

Shibasaki, Kaho,Togo, Hideo

, p. 1816 - 1830 (2020/11/19)

Successive treatment of arenes with acyl chlorides and AlCl3, the addition of water and removal of solvent, the reaction with NH2OH?HCl and K2CO3, and the reaction with diphenylphosphoryl azide and DBU under warming conditions gave the corresponding 5-alkyl-1-aryltetrazoles efficiently in good to moderate yields. The present method is one-pot transformation of arenes into 5-alkyl-1-aryltetrazoles using the Friedel-Crafts acylation and the Beckmann rearrangement under transition-metal-free conditions.

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