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623564-42-1

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623564-42-1 Usage

General Description

8H-Imidazo[2,1-c][1,4]oxazine-2-carboxaldehyde, 5,6-dihydro- (9CI) is a chemical compound with the molecular formula C9H7NO2. It is a heterocyclic compound containing an imidazo[2,1-c][1,4]oxazine ring system with a carboxaldehyde functional group. 8H-Imidazo[2,1-c][1,4]oxazine-2-carboxaldehyde, 5,6-dihydro- (9CI) has potential applications in pharmaceuticals, as it exhibits biological activities such as anti-proliferative and anticancer properties. It can also be used as a chemical intermediate in the synthesis of other organic compounds. Additionally, it may have uses in the field of materials science and chemical research due to its unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 623564-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,3,5,6 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 623564-42:
(8*6)+(7*2)+(6*3)+(5*5)+(4*6)+(3*4)+(2*4)+(1*2)=151
151 % 10 = 1
So 623564-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O2/c10-4-6-3-9-1-2-11-5-7(9)8-6/h3-4H,1-2,5H2

623564-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,8-dihydro-5H-imidazo[2,1-c][1,4]oxazine-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5,6-dihydro-8h-imidazo[2,1-c][1,4]oxazine-2-carbaldehyde

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:623564-42-1 SDS

623564-42-1Relevant articles and documents

Processes For Preparing Bicyclic Oxazine Carboxaldehyde and Beta-Lactamase Inhibitors

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Page/Page column 14, (2009/01/24)

The invention relates to processes for the preparation of the bicyclic oxazine carboxaldehyde Compound 1: The invention also relates to the use of Compound 1 in the preparation of □-lactamase inhibitors.

Bicyclic 6-alkylidene-penems as class-D beta-lactamases inhibitors

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Page/Page column 17-18, (2010/11/25)

This invention relates to certain bicyclic 6-alkylidene penems which act as a inhibitor of class-D enzymes. β-Lactamases hydrolyze β-lactam antibiotics, and as such serve as the primary cause of bacterial resistance. The compounds of the present invention when combined with β-lactam antibiotics will provide an effective treatment against life threatening bacterial infections. In accordance with the present invention there are provided compounds of general formula I or a pharmaceutically acceptable salt or in vivo hydrolyzable ester R5 thereof: wherein: One of A and B denotes hydrogen and the other an optionally substituted fused bicyclic heteroaryl group; and X═O or S.

BICYCLIC 6-ALKYLIDENE-PENEMS AS ?-LACTAMASES INHIBITORS

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Page/Page column 65-66, (2008/06/13)

The present invention provides a compound of Formula (I), pharmaceutical compositions and the use thereof for the treatment of bacterial infection or disease in a patient in need thereof.

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