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1823-76-3

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1823-76-3 Usage

Description

2-hydroxyimino-1-(4-methoxyphenyl)ethanone, also known as carvacrol oxime, is a chemical compound with a molecular formula C10H11NO2. It is derived from carvacrol, a natural compound found in oregano and other plants. This versatile compound possesses antibacterial, antifungal, and antioxidant properties, making it a valuable asset in various industries.

Uses

Used in Pharmaceutical Industry:
2-hydroxyimino-1-(4-methoxyphenyl)ethanone is used as an active pharmaceutical ingredient for its potential therapeutic effects in treating infections and inflammatory conditions. Its natural origin and broad-spectrum antimicrobial activity contribute to its appeal in developing new drugs for various health applications.
Used in Food Industry:
In the food industry, 2-hydroxyimino-1-(4-methoxyphenyl)ethanone is used as a food additive for its preservative qualities. Its ability to inhibit the growth of bacteria and fungi helps maintain the freshness and safety of various food products, extending their shelf life and improving overall food quality.
Used in Drug Development:
2-hydroxyimino-1-(4-methoxyphenyl)ethanone is utilized in the research and development of new drugs, capitalizing on its potential to combat infections and inflammation. Its multifaceted properties allow for exploration in various therapeutic areas, offering promising avenues for novel drug discovery.
Used in Antioxidant Formulations:
As an antioxidant, 2-hydroxyimino-1-(4-methoxyphenyl)ethanone is used in various formulations to protect against oxidative stress and related conditions. Its capacity to neutralize free radicals and reduce oxidative damage makes it a valuable component in health supplements and skincare products.

Check Digit Verification of cas no

The CAS Registry Mumber 1823-76-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1823-76:
(6*1)+(5*8)+(4*2)+(3*3)+(2*7)+(1*6)=83
83 % 10 = 3
So 1823-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO3/c1-13-8-4-2-7(3-5-8)9(11)6-10-12/h2-6,12H,1H3

1823-76-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxyimino-1-(4-methoxyphenyl)ethanone

1.2 Other means of identification

Product number -
Other names Benzeneacetaldehyde,4-methoxy-a-oxo-,1-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:1823-76-3 SDS

1823-76-3Relevant articles and documents

Arylglyoxal oximes as putative C-nucleophiles in eliminative nucleophilic substitution process

Tsyganov, Dmitry V.,Samet, Alexander V.,Dorovatovskii, Pavel V.,Khrustalev, Victor N.,Semenov, Victor V.

, p. 296 - 298 (2019/06/13)

Reaction of arylglyoxal oximes ArCOCH=NOH (Ar = 4-MeOC6H4, Ph) with 5-arylfurazanopyrazines proceeds as vicarious nucleophilic substitution of hydrogen in pyrazine ring with the elimination of hyponitrous acid, affording 5-(aroylmethylidene)-6-aryl-4H-furazano[3,4-b]pyrazines. Structure of the product was confirmed by X-ray diffraction.

Palladium-Catalyzed Direct Arylation of Azine and Azole N-Oxides: Reaction Development, Scope and Applications in Synthesis

Campeau, Louis-Charles,Stuart, David R.,Leclerc, Jean-Philippe,Bertrand-Laperle, Megan,Villemure, Elisia,et al.

supporting information; experimental part, p. 3291 - 3306 (2009/07/30)

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One-pot synthesis of 3-amino-4-aryl- and 3-amino-4-hetarylfurazans

Sheremetev

, p. 1057 - 1059 (2007/10/03)

A "one pot" method for the synthesis of 3-amino-4-aryl- and 3-amino-4-hetarylfurazans from β-aryl- and 4-β-hetaryl-β-oxo acid esters was developed.

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