16303-14-3 Usage
Chemical class
Heterocyclic compound
Explanation
1,3-Benzoxazepine, 2-phenylis a compound that contains a benzene ring fused to an oxazepine ring, making it a heterocyclic compound.
Explanation
At room temperature, 1,3-Benzoxazepine, 2-phenylis a solid with a white to off-white color.
Explanation
The compound does not dissolve well in water, making it insoluble.
Explanation
1,3-Benzoxazepine, 2-phenylis used in the pharmaceutical industry for the synthesis of various drugs, including antidepressants, antipsychotics, and anti-anxiety medications.
Explanation
Studies have shown that 1,3-Benzoxazepine, 2-phenylhas potential biological activities, such as its role in modulating the central nervous system and acting as an anti-inflammatory agent.
Explanation
Due to its unique chemical structure, 1,3-Benzoxazepine, 2-phenylmay have potential applications in the fields of materials science and organic chemistry.
Appearance
White to off-white solid
Solubility
Insoluble in water
Pharmaceutical applications
Synthesis of drugs
Biological activities
Modulating the central nervous system and anti-inflammatory properties
Potential applications
Materials science and organic chemistry
Check Digit Verification of cas no
The CAS Registry Mumber 16303-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,0 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16303-14:
(7*1)+(6*6)+(5*3)+(4*0)+(3*3)+(2*1)+(1*4)=73
73 % 10 = 3
So 16303-14-3 is a valid CAS Registry Number.
16303-14-3Relevant academic research and scientific papers
Reaction of 1,2,4-triazine 1-oxides with benzyne : Formation of 1,3-benzoxazepine and 1,3,5,6-benzoxatriazonine derivatives
Kakusawa, Naoki,Sakamoto, Kazunori,Kurita, Jyoji,Tsuchiya, Takashi
, p. 2091 - 2094 (2007/10/03)
Reaction of the 6-unsubstituted 1,2,4-triazine 1-oxides (5) with benzyne gave the 1,3-benzoxazepines (8) and / or the 6-(o-hydroxyphenyl)-1,2,4-triazines (10) via the unisolable 1,3-dipolar cycloadducts (6), whereas the 6-substituted compound (12), 5,6-dimethyl-3-methoxy-1,2,4-triazine 1-oxide, afforded only the relatively stable 1,5-shift product (15) derived from the initially formed 1,3-dipolar cycloadduct (13). Heating the adduct (15) gave the novel 1,3,5,6-benzoxatriazonine derivative (16) and 2,3-dimethylbenzofuran (17).
ETUDE DE LA REACTIVITE DE L'ION AZOTURE VIS A VIS DE CATIONS HETEROCYCLIQUES-IV COMPORTEMENT VIS A VIS DE CATIONS CHROMYLIUM DIVERSEMENT SUBSTITUES. REARRANGEMENT THERMIQUE DES AZIDES COVALENTS OBTENUS. VOIE ORIGINALE D'ACCES AUX BENZHETEROAZEPINES
Desbene, P.-L.,Cherton, J.-C.
, p. 3567 - 3577 (2007/10/02)
The study of the azide nucleophile reaction with substituted chromylium salts is presented.When heated, the azido 2H-and azdo 4H-chromenes obtained give benz(f)oxazepins in very good yields.This is an easy preparation of these compounds.
