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1-Benzyl-1,4-diazepan-5-one is an organic compound belonging to the diazepane class, characterized by its fused five-membered nitrogen-containing rings. It is a synthetic intermediate with potential applications in the pharmaceutical industry due to its unique chemical structure and properties.

55186-89-5

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55186-89-5 Usage

Uses

1-Benzyl-1,4-diazepan-5-one is used as a chemical intermediate for the synthesis of various pharmaceutical compounds, particularly those with potential therapeutic applications.
Used in Pharmaceutical Industry:
1-Benzyl-1,4-diazepan-5-one is used as a diazepane intermediate for the development of novel drugs targeting specific medical conditions.
Used in Inhibitor Applications:
1-Benzyl-1,4-diazepan-5-one is used as an inhibitor of human nitric oxide synthesis, which can be beneficial in the treatment of conditions where nitric oxide overproduction is a concern, such as certain inflammatory diseases or cardiovascular disorders. By inhibiting nitric oxide synthesis, 1-Benzyl-1,4-diazepan-5-one may help regulate the balance of this important signaling molecule in the body, potentially leading to improved patient outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 55186-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,8 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55186-89:
(7*5)+(6*5)+(5*1)+(4*8)+(3*6)+(2*8)+(1*9)=145
145 % 10 = 5
So 55186-89-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2O/c15-12-6-8-14(9-7-13-12)10-11-4-2-1-3-5-11/h1-5H,6-10H2,(H,13,15)

55186-89-5SDS

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-Benzyl-1,4-diazepan-5-one

1.2 Other means of identification

Product number -
Other names 1-benzylhexahydro-1H-1,4-diazepin-5-one

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:55186-89-5 SDS

55186-89-5Relevant academic research and scientific papers

NOVEL TRIAZINE COMPOUNDS

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Page/Page column 124, (2014/02/16)

The present invention relates to novel triazine compounds of formula (1). The present invention also discloses compounds of formula I along with other pharmaceutical ac-ceptable excipients and use of the compounds to modulate the PI3K/ mTOR pathway

NOVEL TRIAZINE COMPOUNDS

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Page/Page column 73, (2012/08/08)

The present invention relates to novel triazine compounds of formula (1), methods of their preparation, pharmaceutical compositions containing these compounds and the use of these compounds to treat proliferative disorders such as tumors and cancers and also other conditions and disorders related to or associated with dysregulation of PI3 Kinases, PI3 Kinase pathway, mTOR and/ or the mTOR pathway.

PYRAZOLE DERIVATIVE

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Page/Page column 72, (2008/06/13)

Not available

2-chloro-1,3-dimethylimidazolinium chloride. 3. Utility for chlorination, oxidation, reduction, and rearrangement reactions

Isobe, Toshio,Ishikawa, Tsutomu

, p. 5832 - 5835 (2007/10/03)

2-Chloro-1,3-dimethylimidazolinium chloride (1), which can act as a powerful dehydrating equivalent to DCC (2), is also applicable to chlorination, oxidation, reduction, and rearrangement under nearly neutral conditions. The utility of 1 for these reactions is described.

New synthesis of (±)-2-piperazinecarboxylic acid

Merour,Coadou

, p. 2469 - 2470 (2007/10/02)

(±)-2-Piperazinecarboxylic acid is prepared from N-carbethoxy-4-piperidone by α Schmidt rearrangement followed by bromation of the lactam; then α Favorskii rearrangement on the monobromolactam intermediate afforded the desired product.

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