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1,4-Benzoxazepin-5(2H)-one, 3,4-dihydro-4-methyl- is a chemical compound with the molecular formula C10H11NO2. It belongs to the class of benzoxazepinones, which are heterocyclic compounds containing a benzene ring fused to an oxazepine ring. This specific compound features a 3,4-dihydro structure, indicating the presence of two hydrogen atoms in the 3 and 4 positions, and a methyl group attached to the 4 position. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound is also known for its potential applications in the development of novel therapeutic agents targeting central nervous system disorders.

708-05-4

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708-05-4 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. Heterocyclic compound

Explanation

A heterocyclic compound is a cyclic compound that contains atoms of at least two different elements, in this case, carbon, oxygen, and nitrogen.
3. Benzene ring fused to an oxazepine ring

Explanation

The compound's structure consists of a benzene ring (a six-membered ring with alternating single and double bonds) fused to an oxazepine ring (a seven-membered ring containing oxygen and nitrogen atoms).
4. Derivative of benzodiazepine

Explanation

The compound is derived from the benzodiazepine class of chemicals, which are known for their anxiolytic, sedative, and hypnotic properties.
5. Anxiolytic and sedative properties

Explanation

The compound is known to have anxiolytic (anxiety-reducing) and sedative (calming) effects, making it potentially useful in the treatment of anxiety and related disorders.
6. Used in the synthesis of pharmaceuticals

Explanation

The compound serves as a building block or intermediate in the production of various pharmaceutical drugs.
7. Potential applications in medicine

Explanation

Due to its anxiolytic and sedative properties, the compound may have potential uses in the medical field, particularly in the treatment of anxiety and related disorders.
8. Central nervous system effects

Explanation

The compound is being studied for its potential effects on the central nervous system, which could provide insights into its therapeutic applications and mechanisms of action.

Check Digit Verification of cas no

The CAS Registry Mumber 708-05-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 708-05:
(5*7)+(4*0)+(3*8)+(2*0)+(1*5)=64
64 % 10 = 4
So 708-05-4 is a valid CAS Registry Number.

708-05-4Downstream Products

708-05-4Relevant academic research and scientific papers

Facile synthesis of 5-To 7-membered benzolactam compounds via strongly facilitated electrophilic aromtic substitution reaction

Kurouchi, Hiroaki,Otani, Yuko,Ohwada, Tomohiko

, p. 705 - 713 (2017/04/10)

We employed our system to activate aromatic ring-Tethered carbamate compounds with trifluoromethanesulfonic acid to obtain benzolactams with 5-To 7-membered rings, and examined the substrate scope and limitations of this activation method. In 5-membered ring formation, a halogen group on the aromatic ring did not greatly affect the reaction yield, but other electron-donating groups inhibited the cyclization reaction, and various side-reactions occurred. In 7-membered ring formation, eletron-donating groups on aromatic ring promoted the cyclization reaction, but cyclization of electron-deficient aromatic rings did not proceed well. The 6-membered ring formation reaction showed the greatest substrate generality.

Synthesis of Chiral Dibenzo-1,8-diaza-14-crown-4, Dibenzo-1,9-diaza-16-crown-4, and Dibenzo-1,10-diaza-18-crown-4 Ethers by Aromatic Nucleophilic Substitution. Application to the Preparation of Bicyclic Chiral Crown-LiI Complexes

Schultz, Arthur G.,Pinto, Donald J. P.,Welch, Martha

, p. 1372 - 1380 (2007/10/02)

New methods for the preparation od dibenzo-1,8-diaza-14-crown-4, dibenzo-1,9-diaza-16-crown-4, and dibenzo-1,10-diaza-18-crown-4 ethers 2, 4, 5, 14, 15 and 16 are described.Bimolecular cyclization of ortho-substituted benzamides (derived from 1,2-, 1,3-,

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