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2-Thiazoleacetic acid, 4,5-dihydro-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

43183-24-0

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43183-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 43183-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,1,8 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 43183-24:
(7*4)+(6*3)+(5*1)+(4*8)+(3*3)+(2*2)+(1*4)=100
100 % 10 = 0
So 43183-24-0 is a valid CAS Registry Number.

43183-24-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(4,5-dihydro-1,3-thiazol-2-yl)acetate

1.2 Other means of identification

Product number -
Other names 2-Thiazoleacetic acid,4,5-dihydro-,ethyl ester

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:43183-24-0 SDS

43183-24-0Relevant academic research and scientific papers

Easy access to 2-alkyl and 2-arylthiazolines using a modified heteropolyacid catalysis: Application to the synthesis of bacillamide A

Fache,Cros,Piva,Lefebvre

experimental part, p. 2098 - 2109 (2012/06/04)

A straightforward access to 2-alkyl and 2-arylthiazolines by condensation of-aminothiols on nitriles, catalyzed by phosphotungstic acid (2%) under microwave irradiation, is described. This method has been directly applied to a short and efficient synthesi

New carboxylic acid amides of the pyrrole series: Synthetic routes and biological aspects

Walter, Harald

scheme or table, p. 351 - 362 (2009/01/31)

Complex II inhibitors play an important role in agrochemical fungicide research and have been known for more than 40 years. With the introduction of ortho-substituted heterocyclic amides, a breakthrough in activity level and spectrum within this class was achieved. In the meantime all major agrochemical companies have entered this field. In this paper, a special complex II subclass, the pyrrole carboxamides, will be introduced in more detail and the synthesis of selected compounds as well as a short biological SAR analysis of the pyrrole subclass will be discussed.

Studies on Amino Acid Derivatives. Part 7. General Method for the Synthesis of Penam and Cepham and Their Substituted Derivatives

Chiba, Takuo,Sakaki, Jun-ichi,Takahashi, Takumi,Aoki, Kumi,Kamiyama, Akiko,et al.

, p. 1845 - 1852 (2007/10/02)

Penam (7-oxo-4-thia-1-azabicycloheptane), a basic skeleton of penicillin-type β-lactams, has been synthesized as a stable compound from thiazolidinylacetic acid.The key step in this synthesis is the formation of the β-lactam ring by Mukaiyama-Ohno's procedure.Three methods are developed for the synthesis of thiazolidinylacetic acid from cysteamine by reactions with ethyl propiolate, ethyl ethoxycarbonylacetimidate, or t-butyl formylacetate.Using appropriate derivatives of the latter compounds, 5-, 6-, and 5,6-substituted derivatives of penam are also synthesized.The yields of the bicyclic β-lactams are shown to be strongly dependent upon the pattern of substituents on the thiazolidinylacetic acid.The synthesis of cephams using homocysteamine is also described.

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