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10576-12-2

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10576-12-2 Usage

Chemical Properties

clear colorless liquid after melting

Uses

Different sources of media describe the Uses of 10576-12-2 differently. You can refer to the following data:
1. Ethyl N-hydroxyacetimidate was used in the synthesis of O-acyl-and O-nitrophenylhydroxylamines, hydroxamic acid ethoxycarbonylhydrazides and ethyl O-(2,4-dinitrophenyl)acetohydroxamate.
2. Ethyl acetohydroxamate was used in the synthesis of:O-acyl-and O-nitrophenylhydroxylamineshydroxamic acid ethoxycarbonylhydrazidesethyl O-(2,4-dinitrophenyl)acetohydroxamate

Synthesis Reference(s)

Synthesis, p. 220, 1983 DOI: 10.1055/s-1983-30288

Flammability and Explosibility

Flammable

Check Digit Verification of cas no

The CAS Registry Mumber 10576-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,7 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10576-12:
(7*1)+(6*0)+(5*5)+(4*7)+(3*6)+(2*1)+(1*2)=82
82 % 10 = 2
So 10576-12-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NO2/c1-3-7-4(2)5-6/h6H,3H2,1-2H3/b5-4-

10576-12-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Alfa Aesar

  • (A11006)  Ethyl N-hydroxyacetimidate, 97%   

  • 10576-12-2

  • 5g

  • 156.0CNY

  • Detail
  • Alfa Aesar

  • (A11006)  Ethyl N-hydroxyacetimidate, 97%   

  • 10576-12-2

  • 25g

  • 644.0CNY

  • Detail
  • Alfa Aesar

  • (A11006)  Ethyl N-hydroxyacetimidate, 97%   

  • 10576-12-2

  • 100g

  • 2222.0CNY

  • Detail
  • Aldrich

  • (208922)  Ethylacetohydroxamate  97%

  • 10576-12-2

  • 208922-10G

  • 530.01CNY

  • Detail
  • Aldrich

  • (208922)  Ethylacetohydroxamate  97%

  • 10576-12-2

  • 208922-50G

  • 2,159.82CNY

  • Detail

10576-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl acetohydroxamate

1.2 Other means of identification

Product number -
Other names Ethyl N-Hydroxyacetimidate

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:10576-12-2 SDS

10576-12-2Related news

Synthesis of novel chalcones through palladium-catalyzed CO cross-coupling reaction of bromo-chalcones with Ethyl acetohydroxamate (cas 10576-12-2) and their antiplasmodial evaluation against Plasmodium falcipuram in vitro08/14/2019

An efficient method for palladium-catalyzed CO cross-coupling of ethyl acetohydroxamate (EAcHO) with 4-bromo-chalcones has been developed to synthesize novel chalcones. The two supporting ligands, namely tBuXPhos (L7), and cataCXium®PIntB (L16) were found to be effective ligands towards the Pd-c...detailed

10576-12-2Relevant articles and documents

Diastereoselectivity and Reactivity in the Diels-Alder Reactions of α-Chloronitroso Ethers

Felber, Helena,Kresze, Guenter,Prewo, Roland,Vasella, Andrea

, p. 1137 - 1146 (2007/10/02)

The structure of the α-chloronitroso ether 1, obtained from the hydroximolactone 2 and tert-butyl hypochlorite (89percent), was established by X-ray crystallographic analysis.The cycloadditions of 1 with dienes 3 and 8-11 led to the N-unsubstituted 3,6-dihydro-2H-1,2-oxazines 6 and 12-16 in high enantiomeric excess (Table 1).Due to the additional α-alkoxy group, the reactivity of 2 is much superior to the one of known α-chloronitrosoalkanes.The reactive conformation of 1 was deduced from the X-ray analysis as well as the high diastereoselectivity of the cycloadditions.The importance of the α-alkoxy group was evidenced from the similar reactivity of the racemic α-chloronitroso ethers 25-27 which were prepared from the hydroximo ethers 28-30 and tert-butyl hypochlorite.

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