324767-41-1 Usage
Pentadienoic acid derivative
The compound is derived from pentadienoic acid, which is a five-carbon carboxylic acid with two double bonds between the carbons.
Unique molecular structure
The compound has a special structure in which a carbonyl amino group is attached to the 5th carbon of the pentadienoic acid chain.
Carbonyl amino group
This is a functional group that consists of a carbonyl (C=O) group attached to an amino (NH2) group.
(2Z,4E)-isomer
This indicates the geometric isomerism of the compound, with the double bonds at the 2nd and 4th carbons being in the Z (zigzag) and E (straight) configurations, respectively.
Carboxylic acid
The compound is classified as a carboxylic acid, which is a type of acid with a carboxyl (COOH) functional group.
Used in chemical and pharmaceutical research
The compound is commonly used in research due to its unique structure and properties.
Potential applications in drug development
The compound may have potential uses in the development of new drugs and therapeutic compounds, but further research is needed to fully understand its potential uses and effects.
Check Digit Verification of cas no
The CAS Registry Mumber 324767-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,4,7,6 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 324767-41:
(8*3)+(7*2)+(6*4)+(5*7)+(4*6)+(3*7)+(2*4)+(1*1)=151
151 % 10 = 1
So 324767-41-1 is a valid CAS Registry Number.
324767-41-1Relevant articles and documents
A short stereoselective preparation of dienamides from cyclobutene compounds. Application in the synthesis of a new cyclohexene nucleoside
Gauvry,Huet
, p. 583 - 588 (2001)
A short stereoselective synthesis of N-acylamino-1,3-dienes was developed starting from the cyclobutene lactani 8, which was obtained from 2-hydroxypyridine by a photochemical electrocyclic reaction. The tert-butoxycarbonyl derivative 17 was prepared to facilitate nucleophilic attacks to the Carbonyl group, and the subsequent thermal ring opening provided dienes 18-21. One of these (20) was used in the synthesis of the cyclohexene nucleoside 30. A Diels-Alder reaction between diene 20 and maleic anhydride provided the endo-cycloadduct 22a. Three additional steps yielded amine 26. Construction of the uracil moiety afforded intermediate 29. Cyclization and removal of the protecting groups occurred in one step in the presence of ammonia, giving the target molecule 30. Diene 20 also underwent [4 + 2] cycloaddition with methyl acrylate to provide predominantly the endo-product 23a, regioselectively.
