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4-Acetamidobenzenaldehyde oxime is an organic compound with the chemical formula C8H8N2O2. It is a derivative of acetanilide, where the hydroxyl group is replaced by an oxime group. 4-ACETAMIDOBENZALDEHYDE OXIME is characterized by its yellow crystalline appearance and is soluble in common organic solvents such as ethanol and acetone. It is synthesized by the reaction of 4-aminobenzaldehyde with acetic anhydride, followed by the addition of hydroxylamine to form the oxime. 4-Acetamidobenzenaldehyde oxime is used as an intermediate in the synthesis of various pharmaceuticals and dyes, particularly those requiring a benzaldehyde structure with an acetamide and oxime functional group. Its chemical properties make it a valuable building block in organic chemistry, particularly in the preparation of compounds with potential medicinal applications.

5351-33-7

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5351-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5351-33-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5351-33:
(6*5)+(5*3)+(4*5)+(3*1)+(2*3)+(1*3)=77
77 % 10 = 7
So 5351-33-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O2/c1-7(12)11-9-4-2-8(3-5-9)6-10-13/h2-6,13H,1H3,(H,11,12)/b10-6+

5351-33-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-(hydroxyiminomethyl)phenyl]acetamide

1.2 Other means of identification

Product number -
Other names 4-acetylaminobenzaldehyde oxime

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:5351-33-7 SDS

5351-33-7Upstream product

5351-33-7Relevant academic research and scientific papers

Cascade Process for Direct Transformation of Aldehydes (RCHO) to Nitriles (RCN) Using Inorganic Reagents NH2OH/Na2CO3/SO2F2 in DMSO

Fang, Wan-Yin,Qin, Hua-Li

, p. 5803 - 5812 (2019/05/14)

A simple, mild, and practical process for direct conversion of aldehydes to nitriles was developed feathering a wide substrate scope and great functional group tolerability (52 examples, over 90% yield in most cases) using inorganic reagents (NH2OH/Na2CO3/SO2F2) in DMSO. This method allows for transformations of readily available, inexpensive, and abundant aldehydes to highly valuable nitriles in a pot, atom, and step-economical manner without transition metals. This protocol will serve as a robust tool for the installation of cyano-moieties to complicated molecules.

Iodine(III)-Mediated [3 + 2] cyclization for one-pot synthesis of benzo[ d ]isoxazole-4,7-diols in aqueous medium

Hou, Yingwei,Lu, Shichao,Liu, Gang

, p. 8386 - 8395 (2013/09/24)

A one-pot [3 + 2] cycloadditive synthesis of benzo[d]isoxazole-4,7-diols in aqueous medium was carried out via nitrile oxides and benzoquinone intermediates by taking advantage of iodobenzene diacetate as an oxidant. This method can also be used to synthesize benzodiisoxazole-4,8-diols, isoxazolo[5,4-a]phenazines, and indazole-4,7-diols, which are difficult to obtain by classical methods.

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