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Benzenecarboximidic acid, N-hydroxy-, ethyl ester, also known as ethyl N-hydroxybenzenecarboximidate, is organic an compound with the chemical formula C9H11NO2. It is a derivative of benzenecarboximidic acid, where the N-hydroxy group is attached to the benzene ring, and an ethyl ester group is present. Benzenecarboximidic acid, N-hydroxy-, ethyl ester is a colorless liquid with a molecular weight of 165.19 g/mol. It is used as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. Due to its reactivity, it is important to handle Benzenecarboximidic acid, N-hydroxy-, ethyl ester with care, following proper safety protocols.

2446-52-8

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2446-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2446-52-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,4 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2446-52:
(6*2)+(5*4)+(4*4)+(3*6)+(2*5)+(1*2)=78
78 % 10 = 8
So 2446-52-8 is a valid CAS Registry Number.

2446-52-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-hydroxyiminobenzoate

1.2 Other means of identification

Product number -
Other names syn-O-Ethyl-benzhydroxamsaeure

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:2446-52-8 SDS

2446-52-8Relevant academic research and scientific papers

Thermal rearrangement of sugar lactoxime O-vinyl ethers

Yokoyama,Sujino,Irie,Togo

, p. 7269 - 7272 (2007/10/02)

The thermal reaction of sugar lactoxime O-vinyl ethers gave the corresponding 1,3-oxazoles bearing sugar moiety (ribose, glucose, mannose, and maltose) via a novel rearrangement. The reaction mechanism was briefly discussed.

Process for the preparation of organo N-hydroxyimidates

-

, (2008/06/13)

Organo N-hydroxyimidates are prepared by reacting an organonitrile with an organic alcohol and with a hydrogen halide, in the presence of an organic solvent (which may include an excess of the organonitrile reactant), under anhydrous conditions, to form the corresponding organoimidate hydrohalide, and then reacting said organoimidate hydrohalide with a hydroxylamine salt and ammonia gas in the presence of an organic solvent (which can be the excess organonitrile from the first step), under anhydrous conditions, to produce the corresponding organo N-hydroxyimidate.

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