7770-25-4 Usage
Molecular structure
The compound has a triaza-1-azoniatricyclo[3.3.1.1~3,7~]decane core with a 4-methoxyphenyl group attached to the carbon chain.
Classification
It is a quaternary ammonium compound.
Chemical and pharmaceutical applications
The compound is commonly used in various chemical and pharmaceutical applications.
Use as a reactant
It is often used as a reactant in organic synthesis.
Use as a catalyst
The compound can also be utilized as a catalyst for certain chemical reactions.
Unique molecular structure
The compound's unique molecular structure and functional groups make it valuable for a variety of research and industrial purposes.
Functional groups
The compound contains a 4-methoxyphenyl group and a 2-oxoethyl group.
Molecular weight
The molecular weight of the compound is approximately 296.41 g/mol.
Solubility
The compound is likely to be soluble in polar solvents such as water and methanol due to the presence of the 4-methoxyphenyl group and the triaza-1-azoniatricyclo[3.3.1.1~3,7~]decane core.
Check Digit Verification of cas no
The CAS Registry Mumber 7770-25-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,7 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7770-25:
(6*7)+(5*7)+(4*7)+(3*0)+(2*2)+(1*5)=114
114 % 10 = 4
So 7770-25-4 is a valid CAS Registry Number.
7770-25-4Relevant articles and documents
Synthesis of a New Phorbazole and Its Derivatives
Louglin, Wendy A.,Muderawan, I Wayan,Young, David J.
, (2021/11/30)
Phorbazoles are chlorinated marine alkaloids containing pyrrole, oxazole and phenol ring units, and differ in the number and positions of chlorine atoms. They are isolated from sea sponges and nudibranchs. In this work, a convenient synthetic method leading to a new phorbazole and its derivatives is developed. This synthesis of synthetic phorbazole G and its derivatives is achieved in seven steps in good overall yields of 26-52%. It involves formation of the pyrrole-oxazole skeleton followed by chlorination. The pyrrole-oxazole skeleton is synthesized from pyrrole and substituted acetophenones, and the key step involves cyclodehydration of amide intermediates to give protected oxazoles, followed by hydrolysis.
Investigations into the parallel synthesis of novel pyrrole-oxazole analogues of the insecticide pirate
Loughlin, Wendy A.,Henderson, Luke C.,Elson, Kathryn E.,Murphy, Michelle E.
, p. 1975 - 1980 (2007/10/03)
Investigations into the parallel synthesis of selected analogues of a structurally unique pyrrole-oxazole analogue of the pyrrole insecticide pirate, are reported. Acylaminoketone salts were obtained from ketobromides in moderate to high yields and excell
