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Ethyl 2-({tert-butyl[chloro(phenyl)acetyl]amino}methyl)-1,3-thiazole-4-carboxylate is a complex organic compound with the molecular formula C21H24ClN2O3S. It is characterized by a 1,3-thiazole ring, which is a five-membered heterocyclic ring containing sulfur and nitrogen. The compound features a tert-butyl group, a chlorophenyl group, and an ethyl ester group. The tert-butyl group is a bulky, non-reactive alkyl group that provides steric hindrance, while the chlorophenyl group introduces a chlorine atom attached to a phenyl ring. The ethyl ester group is attached to the carboxylate functionality, indicating that the compound is an ester derivative of a carboxylic acid. This chemical is likely to be used in the synthesis of pharmaceuticals or other organic compounds due to its unique structure and functional groups.

5945-67-5

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5945-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5945-67-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,4 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5945-67:
(6*5)+(5*9)+(4*4)+(3*5)+(2*6)+(1*7)=125
125 % 10 = 5
So 5945-67-5 is a valid CAS Registry Number.

5945-67-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[[tert-butyl-(2-chloro-2-phenylacetyl)amino]methyl]-1,3-thiazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names 1-<5-Methyl-furyl-(2)>-3-methyl-buten-(2)-on-(1)

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:5945-67-5 SDS

5945-67-5Downstream Products

5945-67-5Relevant academic research and scientific papers

Friedel-Crafts Reaction of 2-Methylfuran with Saturated and α,β-Unsaturated Acid Anhydrides

Scholz, Stefan,Marschall-Weyerstahl, Helga,Weyerstahl, Peter

, p. 1935 - 1950 (2007/10/02)

2-Methylfuran (5) reacts with the saturated acid anhydrides 16 - 26 in the presence of SnCl4 to give the 2-acyl-5-methylfurans 37 - 47 selectively.The unsaturated anhydrides 27 - 32, however, yield mixtures which only in the case of senecioic acid anhydride (29) contain the respective primary product 48.Subsequent reactions lead to the addition products 55 (from 27) and 56 (from 29), and to (E,Z)-mixtures of their enol esters 57 - 62 which could partially be separated and assigned. - The olfactory properties of 2, 37 - 48, 50, 52, and 53 were investigated.

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