59939-75-2 Usage
Description
(1,4-diazepan-1-yl)(phenyl)methanone is a chemical compound belonging to the benzodiazepine class, characterized by a molecular formula of C16H18N2O. It features a diazepane ring fused with a phenyl group and a methanone functional group, which contribute to its pharmacological properties.
Uses
Used in Pharmaceutical Industry:
(1,4-diazepan-1-yl)(phenyl)methanone is utilized as a central nervous system depressant for its sedative, hypnotic, and anxiolytic properties. It is commonly prescribed by healthcare professionals for the treatment of anxiety disorders, insomnia, and seizures.
However, due to its potential for abuse and dependence, as well as side effects such as drowsiness, dizziness, and impaired coordination, the use of (1,4-diazepan-1-yl)(phenyl)methanone must be carefully monitored and regulated by healthcare professionals to ensure patient safety and effectiveness.
Check Digit Verification of cas no
The CAS Registry Mumber 59939-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,3 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59939-75:
(7*5)+(6*9)+(5*9)+(4*3)+(3*9)+(2*7)+(1*5)=192
192 % 10 = 2
So 59939-75-2 is a valid CAS Registry Number.
59939-75-2Relevant articles and documents
Benzoylation of dianions: Preparation of monobenzoylated derivatives of symmetrical secondary diamines
Wang, Tao,Zhang, Zhongxing,Meanwell, Nicholas A.
, p. 7661 - 7662 (1999)
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PYRIMIDYL-DI(DIAZASPIRO-ALKANES) WITH ANTIVIRAL ACTIVITY
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Page/Page column 17; 18, (2017/05/10)
The invention relates to novel pyrimidyl-di(diazaspiro-alkane) derivatives of formula (I) or a pharmaceutically acceptable acid additive salt thereof. The compounds exhibit a wide spectrum of antiviral activity against herpes virus, human immunodeficiency
Efficient and continuous monoacylation with superior selectivity of symmetrical diamines in microreactors
Maurya, Ram Awatar,Hoang, Phan Huy,Kim, Dong-Pyo
scheme or table, p. 65 - 68 (2012/03/26)
Efficient and continuous monoacylation of symmetrical diamines performed in microreactors yielded superior selectivity to that predicted by statistical considerations. It is highly valuable that the kinetically controlled product in high yields was achieved without any special catalyst at ambient temperature.
