75726-94-2 Usage
Explanation
The compound consists of 8 carbon atoms, 12 hydrogen atoms, 1 bromine atom, 1 nitrogen atom, and 1 oxygen atom.
Explanation
The compound has a ring structure consisting of six carbon atoms and one nitrogen atom, making it a heterocyclic compound with a seven-membered ring.
Explanation
A bromoacetyl group (BrCH2CO-) is attached to one of the carbon atoms in the azepine ring, contributing to the compound's reactivity and properties.
4. Usage in chemical reactions and organic synthesis processes
Explanation
Due to its unique structure and reactivity, 1H-Azepine, 1-(bromoacetyl)hexahydro(9CI) serves as a valuable building block in the synthesis of various chemicals.
5. Applications in pharmaceuticals, agrochemicals, and fine chemicals
Explanation
The compound is used in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals due to its versatile structure and reactivity.
Explanation
1-(bromoacetyl)hexahydro-1H-azepine has potential pharmaceutical applications because of its various biological activities, which can be harnessed for therapeutic purposes.
Explanation
It is important to handle 1H-Azepine, 1-(bromoacetyl)hexahydro(9CI) with care due to its potential toxicity and reactivity, which may pose risks to human health and the environment.
Molecular structure
Heterocyclic compound with a seven-membered azepine ring
Bromoacetyl group attachment
One of the carbon atoms
Potential pharmaceutical applications
Diverse biological activities
Handling precautions
Potential toxicity and reactivity
Check Digit Verification of cas no
The CAS Registry Mumber 75726-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,2 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75726-94:
(7*7)+(6*5)+(5*7)+(4*2)+(3*6)+(2*9)+(1*4)=162
162 % 10 = 2
So 75726-94-2 is a valid CAS Registry Number.
75726-94-2Relevant academic research and scientific papers
α-Bromodiazoacetamides - a new class of diazo compounds for catalyst-free, ambient temperature intramolecular C-H insertion reactions
Kaupang, Asmund,Bonge-Hansen, Tore
supporting information, p. 1407 - 1413 (2013/08/23)
In this work, we introduce a new class of halodiazocarbonyl compounds, α-halodiazoacetamides, which through a metal-free, ambient-temperature thermolysis perform intramolecular C-H insertions to produce α-halo-β-lactams. When carried out with α-bromodiazoacetamides bearing cyclic side chains, the thermolysis reaction affords bicyclic α-halo-β-lactams, in some cases in excellent yields, depending on the ring size and substitution pattern of the cyclic amide side chains.
Solid phase synthesis of a 1,3,5-trisubstituted pyridinium salt library
Lago, M. Amparo,Nguyen, Thomas T.,Bhatnagar, Pradip
, p. 3885 - 3888 (2007/10/03)
The synthesis of a 1,3,5-trisubstituted pyridinium salt combinatorial array containing two variable groups was accomplished in good yields. This entailed the incorporation of 5-bromonicotinic acid onto the resin, followed by Pd(0) catalyzed Suzuki coupling, then alkylation of the pyridine nitrogen and finally cleavage from the resin. A mix and split scheme was also carried out.
