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6275-81-6

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6275-81-6 Usage

General Description

9H-benzo[b]pyrido[4,3,2-mn]acridin-9-one is a chemical compound often utilized in organic and pharmaceutical chemistry due to its potential properties as an antimicrobial and anti-inflammatory agent. The structure of this compound consists of a benzene ring fused with a pyrido[4,3,2-mn]acridin-9-one, resulting in a polycyclic aromatic system. This particular chemical is known for its fluorescence when exposed to UV light. The synthesis of 9H-benzo[b]pyrido[4,3,2-mn]acridin-9-one involves complex organic chemistry techniques which usually require specialized knowledge in the field. Overall, it is a significant compound due to its potential biochemical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6275-81-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6275-81:
(6*6)+(5*2)+(4*7)+(3*5)+(2*8)+(1*1)=106
106 % 10 = 6
So 6275-81-6 is a valid CAS Registry Number.

6275-81-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-carbamoyl-3-oxo-3,4-dihydroquinoxaline-2-carboxamide

1.2 Other means of identification

Product number -
Other names Ketone, 5-acetamido-4-nitro-2-thienyl isopropyl

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:6275-81-6 SDS

6275-81-6Relevant articles and documents

Synthesis of riboflavines, quinoxalinones and benzodiazepines through chemoselective flow based hydrogenations

Baumann, Marcus,Baxendale, Ian R.,Hornung, Christian H.,Ley, Steven V.,Rojo, Maria Victoria,Roper, Kimberley A.

, p. 9736 - 9759 (2014/08/05)

Robust chemical routes towards valuable bioactive entities such as riboflavines, quinoxalinones and benzodiazepines are described. These make use of modern flow hydrogenation protocols enabling the chemoselective reduction of nitro group containing building blocks in order to rapidly generate the desired amine intermediates in situ. In order to exploit the benefits of continuous processing the individual steps were transformed into a telescoped flow process delivering selected benzodiazepine products on scales of 50 mmol and 120 mmol respectively.

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