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2-({[1-(2-THIENYL)ETHYLIDENE]AMINO}OXY)ACETIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30005-32-4

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30005-32-4 Usage

General Description

2-({[1-(2-thienyl)ethylidene]amino}oxy)acetic acid is a chemical compound with the molecular formula C10H11NO4S. It is a derivative of thienyl and is used as an intermediate in organic synthesis. The compound contains a thiophene ring, which is a sulfur-containing aromatic ring, and an amino group attached to an acetic acid group. It can be used as a building block in the synthesis of pharmaceuticals and other organic compounds. 2-({[1-(2-THIENYL)ETHYLIDENE]AMINO}OXY)ACETIC ACID is also used in research and development in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 30005-32-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,0,0 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 30005-32:
(7*3)+(6*0)+(5*0)+(4*0)+(3*5)+(2*3)+(1*2)=44
44 % 10 = 4
So 30005-32-4 is a valid CAS Registry Number.

30005-32-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-thiophen-2-ylethylideneamino)oxyacetic acid

1.2 Other means of identification

Product number -
Other names -

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:30005-32-4 SDS

30005-32-4Downstream Products

30005-32-4Relevant academic research and scientific papers

Study of the Room-Temperature Synthesis of Oxime Ethers by using a Super Base

Kosmalski, Tomasz,Studzińska, Renata,Daniszewska, Natalia,Ullrich, Ma?gorzata,Sikora, Adam,Marsza??, Micha?,Modzelewska-Banachiewicz, Bo?ena

, p. 551 - 557 (2018/08/17)

In this study, we present a convenient method for the synthesis of oxime ethers by reacting oximes with various chlorides (alkyl, functionalized alkyl, and benzyl) and with the subsequent use of a super base—pulverized potassium hydroxide in DMSO. The reactions take place at room temperature and the products are obtained in high yields. The final products were received within 2 min to 3 h. In addition, the compounds do not require chromatographic separation. The structure elucidation of the titled compounds was performed by using 1H NMR and 13C NMR spectroscopy as well as mass spectrometry. The presented method of synthesis for oxime ethers is environmentally friendly, because neither water cooling or heating of the reaction mixture/solvents (necessary for chromatographic purification) is required. The synthesis can be carried out very easily on a large scale.

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