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3-Chloro-5,6,7,8-tetrahydropyrido[4,3-c]pyridazine is a chemical compound with the molecular formula C9H8ClN3. It belongs to the class of pyrido[4,3-c]pyridazine compounds, which are known for their diverse biological activities and potential pharmaceutical applications. As a chlorinated derivative of tetrahydropyrido[4,3-c]pyridazine, 3-chloro-5,6,7,8-tetrahydropyrido[4,3-c]pyridazine may exhibit similar pharmacological properties, making it a promising candidate for medicinal chemistry research and the development of new drug candidates targeting various diseases.

45882-63-1

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45882-63-1 Usage

Uses

Used in Pharmaceutical Chemistry Research:
3-Chloro-5,6,7,8-tetrahydropyrido[4,3-c]pyridazine is used as a research compound in the field of pharmaceutical chemistry for the development of new drug candidates. Its unique structure and potential biological activities make it an interesting target for further study and exploration.
Used in Medicinal Chemistry:
In the medicinal chemistry industry, 3-chloro-5,6,7,8-tetrahydropyrido[4,3-c]pyridazine is used as a starting material or intermediate in the synthesis of various pharmaceutical agents. Its diverse biological activities and potential pharmacological properties allow for the design and development of novel therapeutic agents targeting a wide range of diseases.
Used in Drug Discovery:
3-Chloro-5,6,7,8-tetrahydropyrido[4,3-c]pyridazine is employed in drug discovery processes as a potential lead compound. Its unique chemical structure and biological activities can be further optimized and modified to enhance its therapeutic potential and selectivity, leading to the development of more effective and safer drugs.
Used in Drug Design:
In the field of drug design, 3-chloro-5,6,7,8-tetrahydropyrido[4,3-c]pyridazine serves as a valuable template for the creation of new chemical entities. Its structural features can be exploited to design drugs with improved pharmacokinetic and pharmacodynamic properties, as well as reduced side effects and toxicity.
Overall, 3-chloro-5,6,7,8-tetrahydropyrido[4,3-c]pyridazine is a versatile and promising compound in the realm of pharmaceutical chemistry, with potential applications in research, drug discovery, and drug design. Its unique properties and diverse biological activities make it an attractive target for further exploration and development in the quest for novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 45882-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,8,8 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 45882-63:
(7*4)+(6*5)+(5*8)+(4*8)+(3*2)+(2*6)+(1*3)=151
151 % 10 = 1
So 45882-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H8ClN3/c8-7-3-5-4-9-2-1-6(5)10-11-7/h3,9H,1-2,4H2

45882-63-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-5,6,7,8-tetrahydropyrido[4,3-c]pyridazine

1.2 Other means of identification

Product number -
Other names FD7033

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:45882-63-1 SDS

45882-63-1Downstream Products

45882-63-1Relevant academic research and scientific papers

3-Hydrazino-cycloalkyl[c]pyridazines

-

, (2008/06/13)

This invention provides aminopyridazine derivatives of formula I, SPC1 wherein R1 is amino, or an EQU1 group, wherein each of R3 and R4 is alkyl of 1 to 4 carbon atoms, or R3 and R4 together with the carbon atom to which they are bound, form a cycloalkylidene radical of 5 to 12 carbon atoms, R2 is hydrogen or methyl, A is a --(CH2)n -- group, Wherein n is 0 or an integer from 1 to 7, or an >N--CO--R5 group, Wherein R5 is alkyl or alkenyl of 1 to 16 carbon atoms, cycloalkyl of 3 to 8 carbon atoms, 1-adamantyl, or a --(CH2)m --R6 group, Wherein m is 0 or an integer from 1 to 4, and R6 is phenyl; phenyl monosubstituted by fluorine, chlorine, bromine, alkyl or alkoxy of 1 to 4 carbon atoms, alkylmercapto of 1 to 4 carbon atoms, or phenyl; phenyl substituted by two or three substituents of the group chlorine, alkyl or alkoxy of 1 to 4 carbon atoms; diphenylmethyl, the phenyl rings of which may be monosubstituted by fluorine, chlorine, bromine, alkyl or alkoxy of 1 to 4 carbon atoms; or naphthyl, Or an --OR7 group, Wherein R7 is alkyl or alkenyl of 1 to 4 carbon atoms, or phenyl, phenylalkyl or phenylalkenyl which may be monosubstituted on the phenyl ring by chlorine, alkyl or alkoxy of 1 to 4 carbon atoms, and in which the alkylene or alkenylene chain is of 1 to 4 carbon atoms, And R8 and R9 are each hydrogen or alkyl of 1 to 4 carbon atoms, And acid addition salts thereof. The invention also provides processes for the production of said compounds. Said compounds and pharmaceutically acceptable acid addition salts thereof are useful as antihypertensive agents.

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