738658-87-2 Usage
Molecular structure
The compound consists of a pyrrole ring with various substituents attached to it, including an acetic acid group at position 2, a hexyl group at position 3, a methoxycarbonyl group at position 4, and a phenylmethyl group at position 1.
Class of compound
It belongs to the class of pyrrole derivatives, which are organic compounds that contain a pyrrole ring.
Potential applications
The compound has potential applications in the field of organic synthesis and pharmaceutical research due to its unique structure and properties.
Biological activities
It may have biological activities and could be used as a building block in the synthesis of more complex molecules.
Molecular weight
313.4
Physical properties
The physical properties of the compound, such as its solubility, melting point, and boiling point, are not provided in the material.
Reactivity
The reactivity of the compound with other chemicals is not provided in the material, but it is likely to have reactivity based on the functional groups present in its structure.
Check Digit Verification of cas no
The CAS Registry Mumber 738658-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,8,6,5 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 738658-87:
(8*7)+(7*3)+(6*8)+(5*6)+(4*5)+(3*8)+(2*8)+(1*7)=222
222 % 10 = 2
So 738658-87-2 is a valid CAS Registry Number.
738658-87-2Relevant academic research and scientific papers
Antiproliferative activity in HL60 cells by tetrasubstituted pyrroles: A structure-activity relationship study
Padron, Jose M.,Tejedor, David,Santos-Exposito, Alicia,Garcia-Tellado, Fernando,Martin, Victor S.,Villar, Jesus
, p. 2487 - 2490 (2007/10/03)
A number of tetrasubstituted pyrrole derivatives have been synthesized and evaluated for their in vitro antiproliferative activities using the human promyelocytic leukemia cell line HL60. Tetrasubstituted pyrroles are obtained by irradiation of a silica g
A diversity-oriented strategy for the construction of tetrasubstituted pyrroles via coupled domino processes
Tejedor, David,Gonzalez-Cruz, David,Garcia-Tellado, Fernando,Marrero-Tellado, Jose Juan,Lopez Rodriguez, Matias
, p. 8390 - 8391 (2007/10/03)
A new microwave-assisted rearrangement of 1,3-oxazolidines scaffolds is the basis for a new, metal-free, direct, and modular construction of tetrasubstituted pyrroles from terminal-conjugated alkynes, aldehydes, and primary amines. This new reaction manif
