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4,7-Dichloro-thieno[2,3-d]pyridazine is a heterocyclic chemical compound with the molecular formula C5H2Cl2N2S. It features a thieno ring fused to a pyridazine ring, with chlorine atoms substituting at the 4 and 7 positions of the thieno ring. 4,7-DICHLORO-THIENO[2,3-D]PYRIDAZINE has demonstrated potential in pharmaceutical research as a drug candidate for treating various diseases and serves as a valuable building block in organic synthesis for creating other chemical compounds. Furthermore, its ability to form coordination complexes with metal ions has made it a useful component in materials science and catalysis.

699-89-8

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699-89-8 Usage

Uses

Used in Pharmaceutical Research:
4,7-Dichloro-thieno[2,3-d]pyridazine is used as a drug candidate for the treatment of various diseases due to its unique chemical structure and potential therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, 4,7-Dichloro-thieno[2,3-d]pyridazine is utilized as a building block to create other chemical compounds, contributing to the development of new molecules with specific applications.
Used in Materials Science:
4,7-Dichloro-thieno[2,3-d]pyridazine is employed in materials science for its ability to form coordination complexes with metal ions, which can be beneficial in the design and synthesis of new materials with tailored properties.
Used in Catalysis:
In the catalysis industry, 4,7-Dichloro-thieno[2,3-d]pyridazine is used to form coordination complexes with metal ions, which can enhance the catalytic activity and selectivity of various chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 699-89-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 699-89:
(5*6)+(4*9)+(3*9)+(2*8)+(1*9)=118
118 % 10 = 8
So 699-89-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H2Cl2N2S/c7-5-3-1-2-11-4(3)6(8)10-9-5/h1-2H

699-89-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,7-Dichlorothieno[2,3-d]pyridazine

1.2 Other means of identification

Product number -
Other names 4,7-dichloro-thieno[2,3-d]pyridazine

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:699-89-8 SDS

699-89-8Relevant academic research and scientific papers

SUBSTITUTED PYRIDINES AND PYRIDAZINES WITH ANGIOGENESIS INHIBITING ACTIVITY

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Page/Page column 37, (2009/03/07)

Substituted pyridines and pyridazines having angiogenesis inhibiting activity and generalized structural formula (I) wherein the ring containing A, B, D, E, and L is phenyl or a nitrogen-containing heterocycle; groups X and Y may be any of a variety of defined linking units; R and R may be defined independent substituents or together may be a ring-defining bridge; ring J may be an aryl, pyridyl, or cycloalkyl group; and G groups may be any of a variety of defined substituents. Pharmaceutical compositions containing these materials, and methods of treating a mammal having a condition characterized by abnormal angiogenesis or hyperpermeability processes using these materials are also disclosed.

COMPOUNDS FOR TREATING PULMONARY HYPERTENSION

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Page/Page column 57, (2008/06/13)

The present invention relates to pharmaceutical compositions and combinations for treating, preventing or managing pulmonary hypertension comprising small molecule heterocyclic pharmaceuticals, and more particularly, substituted pyridines and pyridazines optionally combined with at least one additional therapeutic agent.

Substituted pyridines and pyridazines with angiogenesis inhibiting activity

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, (2010/02/05)

Substituted pyridazines having angiogenesis inhibiting activity and the generalized structural formula wherein the ring containing A, B, D, E, and L is phenyl or a nitrogen-containing heterocycle; groups X and Y may be any of a variety of defined linking units; R1and R2may be defined independent substituents or together may be a ring-defining bridge; ring J may be an aryl, pyridyl, or cycloalkyl group; and G groups may be any of a variety of defined substituents. Pharmaceutical compositions containing these materials, and methods of treating a mammal having a condition characterized by abnormal angiogenesis or hyperpermiability processes using these materials are also disclosed.

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