95207-32-2 Usage
Uses
Used in Pharmaceutical Industry:
Benzamide, N-chloro-N-(3-phenylpropoxy)is used as an intermediate in the synthesis of pharmaceuticals for its unique chemical properties. Its ability to form specific bonds and interactions with other molecules makes it a valuable component in the development of new drugs.
Used in Polymer Industry:
In the polymer industry, Benzamide, N-chloro-N-(3-phenylpropoxy)is used as a monomer or a modifier to enhance the properties of polymers. Its presence in the polymer chain can improve characteristics such as strength, flexibility, and chemical resistance.
Used in Agrochemical Industry:
Benzamide, N-chloro-N-(3-phenylpropoxy)is utilized in the agrochemical industry as a precursor for the synthesis of active ingredients in pesticides or herbicides. Its unique structure allows for the development of compounds with targeted effects on pests or weeds, improving the efficiency and selectivity of these products.
Check Digit Verification of cas no
The CAS Registry Mumber 95207-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,2,0 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95207-32:
(7*9)+(6*5)+(5*2)+(4*0)+(3*7)+(2*3)+(1*2)=132
132 % 10 = 2
So 95207-32-2 is a valid CAS Registry Number.
95207-32-2Relevant academic research and scientific papers
N-Alkoxy-N-acylnitrenium Ions as Possible Intermediates in Intramolecular Aromatic Substitution: Novel Formation of N-Acyl-3,4-dihydro-1H-2,1-benzoxazines and N-Acyl-4,5-dihydro-1H,3H-2,1-benzoxazepine
Glover, Stephen A.,Goosen, Andre,McCleland, Cedric W.,Schoonraad, Johan L.
, p. 2255 - 2260 (2007/10/02)
N-Halogeno-N-alkoxyamides undergo intramolecular aromatic substitution by thermal- or Lewis acid-catalysed heterolysis of the nitrogen-halogen bond.N-Acyl-N-alkoxynitrenium ions are likely intermediates.N-Chloro-N-methoxybiphenyl-2-carboxamide (4) yields N-methoxyphenanthridone (11) quantitatively with AgBF4, while O-2-phenylethyl-N-chlorobenzohydroxamate (19) is converted in good yield into N-benzoyl-3,4-dihydro-1H-2,1-benzoxazine (21) with AgBF4, AgClO4, HgO, and Hg(OAc)2.N-Acetyl-3,4-dihydro-1H-2,1-bezoxazine (22) is formed similarly.O-3-Phenylpropyl-N-chlorobenzohydroxamate (23) cyclises to N-benzoyl-4,5-dihydro-1H,3H-2,1-benzoxazepine (24) with AgBF4.
