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3-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazine-6-carbaldehyde is a complex chemical compound belonging to the pyridothiazine class. Characterized by a carbonyl group at the 6-carbon position, 3-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazine-6-carbaldehyde is known for its potential biological activities and is often utilized in organic synthesis and pharmaceutical research. Its unique structure and reactive carbonyl group make it a valuable building block for the synthesis of various functionalized pyrido[3,2-b][1,4]thiazine derivatives, contributing to drug discovery and development.

443956-16-9

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443956-16-9 Usage

Uses

Used in Pharmaceutical Research:
3-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazine-6-carbaldehyde is used as a versatile building block in pharmaceutical research for the synthesis of functionalized pyrido[3,2-b][1,4]thiazine derivatives. Its unique structure and reactive carbonyl group enable the development of new drugs and therapeutic agents for various diseases and conditions.
Used in Organic Synthesis:
In the field of organic synthesis, 3-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazine-6-carbaldehyde serves as a key intermediate compound. Its reactivity and structural features allow for the creation of a wide range of chemical products, expanding the scope of chemical applications and innovations.
Further Research:
3-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazine-6-carbaldehyde is a promising candidate for the development of new drugs and therapeutic agents. However, additional research is necessary to fully understand and harness its potential, ensuring its effective and safe use in various applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 443956-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,9,5 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 443956-16:
(8*4)+(7*4)+(6*3)+(5*9)+(4*5)+(3*6)+(2*1)+(1*6)=169
169 % 10 = 9
So 443956-16-9 is a valid CAS Registry Number.

443956-16-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-oxo-4H-pyrido[3,2-b][1,4]thiazine-6-carbaldehyde

1.2 Other means of identification

Product number -
Other names -

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:443956-16-9 SDS

443956-16-9Relevant academic research and scientific papers

TRICYCLIC ANTIBIOTICS

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, (2011/04/13)

The invention relates to antibacterial compounds of formula (I) wherein U represents CH or N; W represents CH or N; R1 represents alkoxy, halogen or CN; ring A represents a pyrrolidin-1,3-diyl-, a piperidin-1,3-diyl or a morpholin-2,4-diyl group and B represents CH2; or ring A is selected from the groups drawn below: wherein R2 represents H, F or hydroxymethyl, and B is absent; G represents a group selected from the group consisting of —CH═CH-E, wherein Y1, Y2, Y3 and Z independently represent CH or N; Q represents O or S; and E represents phenyl which is mono- or di-substituted wherein the substituents are each independently halogen; and to pharmaceutically acceptable salts of such compounds.

The design of efficient and selective routes to pyridyl analogues of 3-oxo-3,4-dihydro-2H-1,4-(benzothiazine or benzoxazine)-6-carbaldehydes

Brooks, Gerald,Dabbs, Steven,Davies, David T.,Hennessy, Alan J.,Jones, Graham E.,Markwell, Roger E.,Miles, Timothy J.,Owston, Nathan A.,Pearson, Neil D.,Peng, Tony W.

scheme or table, p. 5035 - 5037 (2011/01/04)

This Letter describes the synthesis of challenging pyridyl analogues of 3-oxo-3,4-dihydro-2H-1,4-(benzothiazine or benzoxazine)-6-carbaldehydes. The six different routes described are high yielding, contain no major purification issues and have been used to give gram quantities of each aldehyde.

5-Quinoline derivatives having an anti-bacterial activity

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Page/Page column 10, (2010/12/31)

The present invention describes novel anti-bacterial compounds of the formula (I). These compounds are, amongst others, of interest as inhibitors of DNA gyrase and topoisomerases, for example of topoisomerase II and IV.

TRICYCLIC ANTIBIOTICS

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, (2009/12/02)

The invention relates to antibacterial compounds of formula (I) wherein U represents CH or N; W represents CH or N; R1 represents alkoxy, halogen or CN; ring A represents a pyrrolidin-l,3-diyl-, a piperidin-l,3-diyl or a morpholin-2,4-diyl group and B represents CH2; or ring A is selected from the groups drawn below:formula (II) wherein R2 represents H, F or hydroxymethyl, and B is absent; G represents a group selected from the group consisting of -CH=CH-E,formula (III) and formula (IV) wherein Y1, Y2, Y3 and Z independently represent CH or N; Q represents O or S; and E represents phenyl which is mono- or di-substituted wherein the substituents are each independently halogen; and to pharmaceutically acceptable salts of such compounds.

Antibacterial Agents

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Page/Page column 11, (2008/12/07)

Naphthalene, quinoline, quinoaline and naphthyridine derivatives useful in the treatment of bacterial infections in mammals, particularly humans, are disclosed herein.

ETHANOL OR 1,2-ETHANEDIOL CYCLOHEXYL ANTIBIOTIC DERIVATIVES

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Page/Page column 48, (2008/06/13)

The invention relates to antibiotic ethanol or 1,2-ethanediol cyclohexyl derivatives of formula (I) wherein R1 represents (C1-C4)alkoxy; one or two of U, V, W and X represent(s) N and the remaining represent each independently CH or, in the case of V or X

ANTIBACTERIAL AGENTS

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Page/Page column 32, (2008/06/13)

2H-chromen-2-one derivatives useful in the treatment of bacterial infections in mammals, particularly humans, are disclosed herein.

ANTIBACTERIAL AGENTS

-

Page/Page column 34, (2010/11/25)

Naphthalene, quinoline, quinoxaline and naphthyridine derivatives useful in the treatment of bacterial infections in mammals, particularly humans, are disclosed herein.

ANTIBACTERIAL AGENTS

-

Page/Page column 21-22, (2008/06/13)

Naphthyridine and related derivatives useful in the treatment of bacterial infections in mammals, particularly humans, are disclosed herein.

ANTIBACTERIAL AGENTS

-

Page/Page column 22, (2008/06/13)

Naphthyridine and related derivatives useful in the treatment of bacterial infections in mammals, particularly humans, are disclosed herein.

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