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3,8-Dichloro-11H-dibenzo[c,f][1,2]diazepin-11-one 5-oxide is a complex organic compound with the molecular formula C14H8Cl2N2O2. It is a derivative of dibenzo[c,f][1,2]diazepine, a tricyclic aromatic compound with a diazepine ring fused to a benzene ring. The presence of two chlorine atoms at the 3 and 8 positions, along with the 11-oxide group, gives 3,8-Dichloro-11H-dibenzo[c,f][1,2]diazepin-11-one 5-oxide unique chemical properties. It is primarily used in the pharmaceutical industry as an intermediate in the synthesis of various drugs, particularly those with anxiolytic, antidepressant, and antipsychotic properties. Due to its complex structure and potential applications, research on 3,8-Dichloro-11H-dibenzo[c,f][1,2]diazepin-11-one 5-oxide and its derivatives is ongoing to explore their therapeutic potential and optimize their pharmacological effects.

960-86-1

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960-86-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 960-86-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 960-86:
(5*9)+(4*6)+(3*0)+(2*8)+(1*6)=91
91 % 10 = 1
So 960-86-1 is a valid CAS Registry Number.

960-86-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,8-dichlorodibenzo<c,f><1,2>diazepin-11-one-5-oxide

1.2 Other means of identification

Product number -
Other names 3,8-Dichlor-11H-dibenzo-<c,f><1,2>-diazepin-11-on-N-oxid

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:960-86-1 SDS

960-86-1Downstream Products

960-86-1Relevant academic research and scientific papers

Photolysis of 2,2'-Dinitrodiphenylcarbinols in Neutral, Acidic and Basic Media

Jacob, E. Dominic,Joshua, C. P.

, p. 811 - 814 (2007/10/02)

Photolysis of various substituted 2,2'-dinitrodiphenylcarbinols (1a-c) has been carried out in 2-propanol, acidified ethanol and triethylamine. 2-Nitro-2'-nitrosobenzophenones (2a-c) are the major products.Small amounts of 3-(2'-nitrophenyl)-2,1-benzisoxa

Photo-Rearrangement of 3-(2'-Nitrophenyl)-2,1-benzisoxazoles - An Example of Neighbouring Group Interaction of Photoexcited Nitro Group

Christudhas, M.,Joshua, C. P.,Ramdas, P. K.

, p. 325 - 327 (2007/10/02)

3-(2'-Nitrophenyl)-2,1-benzisoxazole (2) when irradiated in acidic ethanol affords dibenzodiazepin-11-one-5-oxide (3) and acridone (4). 5-Methyl-3-(5'-methyl-2'-nitrophenyl)-2,1-benzisoxazoles (2d-h) and 5-methyl-3-(3'-methyl-2'-nitrophenyl)-2,1-benzisoxazoles (2i-k) are also found to rearrange into related N-oxides and acridones.A plausible mechanism is suggested for the photoreaction.

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