Welcome to LookChem.com Sign In|Join Free
  • or
6-Chloro-3-cyclopropyl-[1,2,4]triazolo[4,3-b]pyridazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1152552-07-2

Post Buying Request

1152552-07-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1152552-07-2 Usage

Chemical classification

Heterocyclic compound

Chemical structure

Contains a triazolo ring and a chloro substitution on the cyclopropyl group

Family

Pyridazine

Potential pharmacological properties

May have applications in the development of new therapeutic agents

Interest in medicinal chemistry

Potential drug candidate for various diseases and conditions

Check Digit Verification of cas no

The CAS Registry Mumber 1152552-07-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,2,5,5 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1152552-07:
(9*1)+(8*1)+(7*5)+(6*2)+(5*5)+(4*5)+(3*2)+(2*0)+(1*7)=122
122 % 10 = 2
So 1152552-07-2 is a valid CAS Registry Number.

1152552-07-2SDS

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 6-chloro-3-cyclopropyl-[1,2,4]triazolo[4,3-b]pyridazine

1.2 Other means of identification

Product number -
Other names 6-Chloro-3-cyclopropyl-[1,2,4]triazolo[4,3-b]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:1152552-07-2 SDS

1152552-07-2Downstream Products

1152552-07-2Relevant academic research and scientific papers

Kinase domain inhibition of leucine rich repeat kinase 2 (LRRK2) using a [1,2,4]triazolo[4,3-b]pyridazine scaffold

Galatsis, Paul,Henderson, Jaclyn L.,Kormos, Bethany L.,Han, Seungil,Kurumbail, Ravi G.,Wager, Travis T.,Verhoest, Patrick R.,Noell, G. Stephen,Chen, Yi,Needle, Elie,Berger, Zdenek,Steyn, Stefanus J.,Houle, Christopher,Hirst, Warren D.

, p. 4132 - 4140 (2014)

Leucine rich repeat kinase 2 (LRRK2) has been genetically linked to Parkinson's disease (PD). The most common mutant, G2019S, increases kinase activity, thus LRRK2 kinase inhibitors are potentially useful in the treatment of PD. We herein disclose the str

COMPOUNDS AND THEIR METHODS OF USE

-

Page/Page column 125, (2018/06/12)

The present invention is directed to, in part, fused heteroaryl compounds and compositions useful for preventing and/or treating a disease or condition relating to aberrant function of a voltage-gated, sodium ion channel, for example, abnormal late/persistent sodium current. Methods of treating a disease or condition relating to aberrant function of a sodium ion channel including Dravet syndrome or epilepsy are also provided herein.

A Convenient One-Pot Synthesis of Triazolopyridine and Related Heterocycle Fused-Triazole Analogs Through Copper Catalyzed Oxidative Cyclization Strategy

Srinivasan,Sembian Ruso,Nagarajan,Senthil Kumaran,Manickam

, p. 606 - 614 (2016/04/19)

One-pot synthesis of heterocycle fused-triazole analogs from the corresponding aldehydes and heteroarylhydrazines is demonstrated. Transformation of hydrazones to the desired systems was achieved by employing the oxidative cyclization with catalytic CuBr2 and oxone. This reaction condition is mild and selective, and a wide range of functional groups were able to sustain. An array of biologically important triazolopyridines, triazolopyridazines, triazolopyrimidines, and triazoloquinolines were obtained in fairly good yield.

Triazolopyridazine LRRK2 kinase inhibitors

Franzini, Maurizio,Ye, Xiaocong M.,Adler, Marc,Aubele, Danielle L.,Garofalo, Albert W.,Gauby, Shawn,Goldbach, Erich,Probst, Gary D.,Quinn, Kevin P.,Santiago, Pam,Sham, Hing L.,Tam, Danny,Truong, Anh,Ren, Zhao

, p. 1967 - 1973 (2013/04/24)

Leucine-rich repeat kinase 2 (LRRK2) has been implicated in the pathogenesis of Parkinson's disease (PD). Inhibition of LRRK2 kinase activity is a therapeutic approach that may lead to new treatments for PD. Herein we report the discovery of a series of [

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1152552-07-2