7048-98-8 Usage
Complex organic molecule
The compound is a complex organic molecule with a variety of functional groups and structural elements.
Thiazole ring
The compound contains a thiazole ring, which is a five-membered ring with two nitrogen atoms and one sulfur atom.
Dimethylaminoethyl group
The compound has a dimethylaminoethyl group, which is an alkyl chain with an amino group that is substituted with two methyl groups.
Propoxyphenyl group
The compound also contains a propoxyphenyl group, which is a phenyl group that is substituted with a propoxy group.
Hydroxy and carbonyl groups
The compound has a hydroxy group (-OH) and a carbonyl group (C=O), which are important functional groups in organic chemistry.
Potential applications in the pharmaceutical industry
Due to its structural features, the compound may have potential applications in the pharmaceutical industry.
Structural features contributing to pharmacological properties
The compound's structure suggests that it may have biological activity and could be of interest for further research and development.
Synthesis and characterization
The synthesis and characterization of the compound are important for understanding its potential uses and properties.
Biological activity
The compound's structure suggests that it may have biological activity, which could be explored for potential therapeutic applications.
Further research and development
The compound's potential uses and properties warrant further research and development to fully understand its capabilities and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 7048-98-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,4 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7048-98:
(6*7)+(5*0)+(4*4)+(3*8)+(2*9)+(1*8)=108
108 % 10 = 8
So 7048-98-8 is a valid CAS Registry Number.
7048-98-8Relevant articles and documents
Synthesis of [n]- and [n.n]Cyclophanes by using Suzuki-Miyaura coupling
Smith, Beverly B.,Hill, Darron E.,Cropp, T. Ashton,Walsh, Rosa D.,Cartrette, David,Hipps, Sherry,Shachter, Amy M.,Pennington, William T.,Kwochka, William R.
, p. 5333 - 5337 (2007/10/03)
Reaction of the bis-9-BBN adduct of several dienes with 1,3-dibromobenzene via Suzuki coupling leads to a series of [n]metacyclophanes ranging in size from 10 to 17 atom members. In each case, two carbon-carbon bonds are formed in one reaction vessel. However, when the bis-9-BBN adduct of 1,5-hexadiene is coupled with a variety of aryl dihalides, larger [n.n]cyclophanes were formed in preference to the [n]cyclophanes. Four carbon-carbon bonds are formed in this instance. Single-crystal X-ray analyses of these [n.n]cyclophanes reveal interestingly shaped molecules with large cavities.
Cyclophanes, XXI. The Chemical Behavior of Paracyclophane: Reactions of the Benzene Ring
Noble, Karl-Ludwig,Hopf, Henning,Ernst, Ludger
, p. 455 - 473 (2007/10/02)
Preparative quantities of paracyclophane (1b) may be prepared from paracyclophane-3,6-dione (9) by Wolff-Kishner reduction.After a detailed dicussion of the 1H and 13C NMR spectra of 1b, its behavior in substitution and addition reactions is describ
