478951-91-6 Usage
Description
[2-(Acetyloxy)-5-nitro-1,3-phenylene]di(methylene) diacetate, with the molecular formula C14H14N2O10, is a diester chemical compound derived from the acetylation of hydroxy groups of the nitrophenyl ring and dihydroxymethylene groups. It is characterized by its potential applications in various industries, particularly in the synthesis of organic compounds and pharmaceuticals.
Uses
Used in Pharmaceutical Industry:
[2-(Acetyloxy)-5-nitro-1,3-phenylene]di(methylene) diacetate is used as an intermediate for the synthesis of various drugs and active pharmaceutical ingredients. Its unique structure allows for the creation of complex organic molecules, making it a valuable precursor in drug development.
Used in Organic Chemistry:
In the field of organic chemistry, [2-(Acetyloxy)-5-nitro-1,3-phenylene]di(methylene) diacetate serves as a starting material for the synthesis of complex organic molecules. Its versatile chemical properties enable researchers to explore new pathways and create novel compounds with potential applications in various sectors.
Potential Applications in Research and Development:
[2-(Acetyloxy)-5-nitro-1,3-phenylene]di(methylene) diacetate may also possess biological and pharmacological properties, which make it a subject of interest for further research and development. As our understanding of its properties and potential applications grows, it could lead to new discoveries and innovations in the fields of medicine, chemistry, and other related industries.
Check Digit Verification of cas no
The CAS Registry Mumber 478951-91-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,9,5 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 478951-91:
(8*4)+(7*7)+(6*8)+(5*9)+(4*5)+(3*1)+(2*9)+(1*1)=216
216 % 10 = 6
So 478951-91-6 is a valid CAS Registry Number.
478951-91-6Relevant articles and documents
Modification of the upper rim of homooxacalix[3]arenes and complexation between a nitrohomooxacalix[3]arene derivative and n-hexylamine
Tsubaki, Kazunori,Otsubo, Tadamune,Morimoto, Tatsuya,Maruoka, Hiromi,Furukawa, Mika,Momose, Yashima,Shang, Muhong,Fuji, Kaoru
, p. 8151 - 8156 (2007/10/03)
Several functional groups were introduced on the upper rim of (lower rim free) homooxacalix[3]-arene for the first time. The swinging nitrohomooxacalix[3]arene host 1 was fixed in the cone conformation by complexation with n-hexylamine.
