188608-74-4 Usage
Molecular Structure
1H-Pyrrole, 2-[(S)-(4-methylphenyl)sulfinyl]-1-[(2E)-1-oxo-3-phenyl-2-propenyl]is a compound containing a pyrrole ring, a sulfinyl group, and a 1-oxo-3-phenyl-2-propenyl group.
Stereochemistry
The (S)-(4-methylphenyl)sulfinyl group indicates the stereochemistry of the sulfinyl group, which is important for its potential reactivity and biological activity.
Pyrrole Ring
The presence of a pyrrole ring suggests that the compound may have properties similar to other nitrogen-containing heterocyclic compounds, which are commonly found in organic synthesis and biological systems.
Sulfinyl Group
The sulfinyl group (R-S(=O)-) is a functional group that can be involved in various chemical reactions, such as oxidation and reduction processes.
1-Oxo-3-phenyl-2-propenyl Group
This group is a conjugated system with a carbonyl group (C=O) and a vinyl group (C=C), which may contribute to the compound's electronic properties and reactivity.
Organic Synthesis Intermediate
1H-Pyrrole, 2-[(S)-(4-methylphenyl)sulfinyl]-1-[(2E)-1-oxo-3-phenyl-2-propenyl]is a potentially important intermediate in organic synthesis due to its unique structure and functional groups.
Biological Activity
The compound may have biological activity in certain contexts, but further research would be needed to determine its exact properties and potential uses.
Further Research
The compound's exact properties, reactivity, and potential applications in organic synthesis and biological systems require additional investigation to be fully understood.
Check Digit Verification of cas no
The CAS Registry Mumber 188608-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,6,0 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 188608-74:
(8*1)+(7*8)+(6*8)+(5*6)+(4*0)+(3*8)+(2*7)+(1*4)=184
184 % 10 = 4
So 188608-74-4 is a valid CAS Registry Number.
188608-74-4Relevant articles and documents
Recoverable chiral sulfoxide: remote asymmetric induction in Lewis acid-promoted Diels-Alder reaction of chiral sulfinyl-substituted pyrrolyl α,β-unsaturated enones
Arai, Yoshitsugu,Masuda, Tsutomu,Masaki, Yukio
, p. 2165 - 2170 (2007/10/03)
1-[2-(p-Tolylsulfinyl)]pyrrolyl α,β-unsaturated enones served as efficient dienophiles in the Diels-Alder reaction, where the use of aluminium chloride or a lanthanide triflate effected the cycloaddition with cyclopentadiene, affording the endo adduct with high diastereoselectivity. In particular, for the sulfinyl dienophile, the chiral auxiliary (i.e. the sulfinyl pyrrole) was recovered after use without any loss of optical purity.
