135192-15-3 Usage
Explanation
Different sources of media describe the Explanation of 135192-15-3 differently. You can refer to the following data:
1. The compound consists of 9 carbon atoms, 9 hydrogen atoms, 1 nitrogen atom, and 1 oxygen atom.
2. It contains a five-membered ring with one nitrogen atom, making it a heterocyclic compound (containing a ring structure with more than one type of atom).
3. It has a five-membered ring structure with one nitrogen atom, classifying it as a pyrrole.
4. This name is derived from its structure, which includes a 3-butenyl group attached to a pyrrole carboxaldehyde moiety.
5. Due to its pleasant and distinctive odor, it is commonly used in the production of fragrances and flavors.
6. It serves as a building block in organic synthesis, aiding in the creation of more complex molecules.
7. It is used as a precursor in various chemical reactions, particularly in the production of pharmaceuticals.
8. Researchers are exploring its potential use in the field of materials science, possibly for creating new materials with unique properties.
Type of compound
Heterocyclic organic compound
Subtype
Pyrrole compound
Usage in manufacturing
Fragrances and flavors
Application in organic synthesis
Building block
Usage in pharmaceutical production
Precursor in chemical reactions
Potential applications
Materials science
Check Digit Verification of cas no
The CAS Registry Mumber 135192-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,1,9 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 135192-15:
(8*1)+(7*3)+(6*5)+(5*1)+(4*9)+(3*2)+(2*1)+(1*5)=113
113 % 10 = 3
So 135192-15-3 is a valid CAS Registry Number.
135192-15-3Relevant articles and documents
Synthesis of aza polycyclic compounds derived from pyrrolidine, indolizidine, and indole via intramolecular Diels - Alder cycloadditions of neutral 2-azadienes
Palacios, Francisco,Alonso, Concepcion,Amezua, Patricia,Rubiales, Gloria
, p. 1941 - 1946 (2007/10/03)
A method for the preparation of novel oxaza and diaza polycyclic 9-oxa-4-azaphenanthrene, 5H-pyrido[2,3-α]pyrrolizine, 5H,6H-pyrido[3,2-g]indolizine, and 5H,6H-indeno[2,1-α]indole is described, based on tandem reactions: aza-Wittig reaction of N-vinylic phosphazenes with functionalized aldehydes and an intramolecular aza-Diels - Alder reaction.
Thermally Induced Intramolecular Oxime Olefin Cycloadditions (IOOC) Leading to N-Bridgehead Systems. Stereochemistry and Molecular Mechanics Calculations
Hassner, Alfred,Maurya, Rakesh,Padwa, Albert,Bullock, William H.
, p. 2775 - 2781 (2007/10/02)
The intramolecular oxime olefin cycloaddition (IOOC) of proline and pipecolinic acid derivatives proceeds thermally with a high degree of stereoselectivity to provide a new route to functionalized pyrrolizidines, indolizidines, or quinolizidines.The ring closure proceeds with simultaneous stereoselective introduction of three or four stereocenters.Molecular mechanics calculations have been refined to accurately predict not only which stereoisomer is preferred but also the syn and anti coupling constants in these tricyclic molecules.
