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(1Z)-1-(hydroxyimino)-1-phenylpropan-2-one, also known as benzaldehyde oxime or phenylpropionoxime, is a ketoxime derivative with the molecular formula C9H9NO2. It is an organic compound that has been found to possess potential medicinal properties, such as anti-inflammatory, anti-bacterial, and anti-fungal activities.
Used in Pharmaceutical Industry:
(1Z)-1-(hydroxyimino)-1-phenylpropan-2-one is used as a pharmaceutical precursor for the synthesis of other biologically active molecules due to its potential medicinal properties.
Used in Organic Chemistry:
(1Z)-1-(hydroxyimino)-1-phenylpropan-2-one is used as a reagent in the field of organic chemistry for the synthesis of various compounds.

25355-34-4

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25355-34-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25355-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,5 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25355-34:
(7*2)+(6*5)+(5*3)+(4*5)+(3*5)+(2*3)+(1*4)=104
104 % 10 = 4
So 25355-34-4 is a valid CAS Registry Number.

25355-34-4SDS

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 (1E)-1-hydroxyimino-1-phenylpropan-2-one

1.2 Other means of identification

Product number -
Other names 1-oximino-1-phenyl-2-propanone

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:25355-34-4 SDS

25355-34-4Relevant academic research and scientific papers

1,2,5-thiadiazole-2 oxide analogue and application thereof

-

Paragraph 0052; 0053-0056; 0071; 0072; 0073; 0074; 0076, (2017/07/31)

The invention belongs to the field of pharmaceutical chemistry and discloses a 1,2,5-thiadiazole-2 oxide analogue and application thereof. The compound blocks a normal redox equilibrium process of schistosoma cells to kill schistosoma. When the drug conce

Transition-Metal-Free Deacylative Cleavage of Unstrained C(sp3)-C(sp2) Bonds: Cyanide-Free Access to Aryl and Aliphatic Nitriles from Ketones and Aldehydes

Ge, Jing-Jie,Yao, Chuan-Zhi,Wang, Mei-Mei,Zheng, Hong-Xing,Kang, Yan-Biao,Li, Yadong

, p. 228 - 231 (2016/02/03)

A transition-metal-free deacylative C(sp3)-C(sp2) bond cleavage for the synthetically practical oxidative amination of ketones and aldehydes to nitriles is first described, using cheap and commercially abundant NaNO2 as the oxidant and the nitrogen source. Various nitriles bearing aryl, heteroaryl, alkyl, and alkenyl groups could be smoothly obtained from ketones and aldehydes in high yields, avoiding highly toxic cyanides or transition metals.

FACILE DIRECT α-OXIMATION OF KETONES USING t-BUTYL THIONITRATE

Kim, Yong Hae,Park, Young Jun,Kim, Kweon

, p. 2833 - 2836 (2007/10/02)

Various ketones containing methylene groups at α-position were found to react with t-butyl thionitrate at 0 deg C in tetrahydrofuran to give the corresponding α-oximino-ketones in excellent yield.

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