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BENZO[F][1,4]OXAZEPINE-3,5-DIONE is a heterocyclic chemical compound with a molecular formula C13H6N2O3. It belongs to the oxazepine family and features a nitrogen and oxygen atom in its ring structure. Known for its potential pharmaceutical applications, particularly in medicinal chemistry, BENZO[F][1,4]OXAZEPINE-3,5-DIONE is utilized in the synthesis of various drugs and has demonstrated promise in treating different medical conditions. Its distinctive structural properties and reactivity render it a valuable molecule in the fields of organic chemistry and drug discovery research.

14151-88-3

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14151-88-3 Usage

Uses

Used in Pharmaceutical Industry:
BENZO[F][1,4]OXAZEPINE-3,5-DIONE is used as a key intermediate in the synthesis of various pharmaceutical drugs for its unique structural properties and reactivity. It plays a crucial role in the development of new medications targeting a range of medical conditions.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, BENZO[F][1,4]OXAZEPINE-3,5-DIONE is employed as a valuable molecule for drug discovery. Its potential in the treatment of various medical conditions makes it an important compound for designing and developing innovative therapeutic agents.
Used in Organic Chemistry:
BENZO[F][1,4]OXAZEPINE-3,5-DIONE is also utilized in organic chemistry due to its distinctive structural properties and reactivity. It serves as a building block for the creation of complex organic molecules and contributes to the advancement of chemical synthesis techniques.

Check Digit Verification of cas no

The CAS Registry Mumber 14151-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,5 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14151-88:
(7*1)+(6*4)+(5*1)+(4*5)+(3*1)+(2*8)+(1*8)=83
83 % 10 = 3
So 14151-88-3 is a valid CAS Registry Number.

14151-88-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-benzoxazepine-3,5-dione

1.2 Other means of identification

Product number -
Other names Salicylsaeure-O-essigsaeureimid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:14151-88-3 SDS

14151-88-3Relevant academic research and scientific papers

Synthesis, SAR studies, and evaluation of 1,4-benzoxazepine derivatives as selective 5-HT1A receptor agonists with neuroprotective effect: Discovery of Piclozotan

Kamei, Katsuhide,Maeda, Noriko,Nomura, Kayoko,Shibata, Makoto,Katsuragi-Ogino, Ryoko,Koyama, Makoto,Nakajima, Mika,Inoue, Teruyoshi,Ohno, Tomochika,Tatsuoka, Toshio

, p. 1978 - 1992 (2007/10/03)

A new series of 1,4-benzoxazepine derivatives was designed, synthesized, and evaluated for binding to 5-HT1A receptor and cerebral anti-ischemic effect. A lot of compounds exhibited nanomolar affinity for 5-HT1A receptor with good selectivity over both dopamine D 2 and α1-adrenergic receptors. Among these compounds, 3-chloro-4-[4-[4-(2-pyridinyl)-1,2,3,6-tetrahydropyridin-1-yl]butyl]- 1, 4-benzoxazepin-5(4H)-one (50: SUN N4057 (Piclozotan) as 2HCl salt) showed remarkable neuroprotective activity in a transient middle cerebral artery occlusion (t-MCAO) model.

New 5-HT1A receptor agonists possessing 1,4-benzoxazepine scaffold exhibit highly potent anti-ischemic effects.

Kamei,Maeda,Ogino,Koyama,Nakajima,Tatsuoka,Ohno,Inoue

, p. 595 - 598 (2007/10/03)

A series of new 3-substituted-4-(4-aminobutyl)-1,4-benzoxazepin-5(4H)-one derivatives (1-5) which showed a very high affinity for 5-HT1A receptor with good selectivity over dopamine D2 receptor was synthesized. Among these compounds, 3-chloro-4-[4-[4-(2-p

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