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6-Chloro-3-pyridazinecarbonitrile is an organic compound with the chemical formula C6H2ClN3. It is a derivative of pyridazine, a heterocyclic compound consisting of a six-membered nitrogen-containing ring. The presence of a chlorine atom at the 6-position and a nitrile group at the 3-position gives 6-Chloro-3-pyridazinecarbonitrile unique chemical properties and reactivity.

35857-89-7

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35857-89-7 Usage

Uses

Used in Pharmaceutical Industry:
6-Chloro-3-pyridazinecarbonitrile is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a versatile building block for the development of new drugs with potential therapeutic applications.
Used in Synthesis of Stearoyl-CoA Desaturase-1 Inhibitors:
6-Chloro-3-pyridazinecarbonitrile is used as a reactant in the synthesis of spiropiperidine-based stearoyl-CoA desaturase-1 (SCD-1) inhibitors. SCD-1 is an enzyme involved in the synthesis of monounsaturated fatty acids, and its inhibition can have potential applications in the treatment of metabolic disorders such as obesity and diabetes. The incorporation of 6-chloro-3-pyridazinecarbonitrile into the molecular structure of these inhibitors contributes to their biological activity and selectivity towards the target enzyme.

Check Digit Verification of cas no

The CAS Registry Mumber 35857-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,5 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35857-89:
(7*3)+(6*5)+(5*8)+(4*5)+(3*7)+(2*8)+(1*9)=157
157 % 10 = 7
So 35857-89-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H2ClN3/c6-5-2-1-4(3-7)8-9-5/h1-2H

35857-89-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloropyridazine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 6-Chlor-pyridazin-3-carbonitril

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:35857-89-7 SDS

35857-89-7Relevant academic research and scientific papers

NOVEL TRIFLUOROMETHYL-OXADIAZOLE DERIVATIVES AND THEIR USE IN THE TREATMENT OF DISEASE

-

Page/Page column 68, (2013/06/27)

The invention relates to novel trifluoromethyl-oxadiazole derivatives of formula (I), and pharmaceutically acceptable salts thereof, in which all of the variables are as defined in the specification, pharmaceutical compositions thereof, pharmaceutical com

PIPERIDINYLAMINO-PYRIDAZINES AND THEIR USE AS FAST DISSOCIATING DOPAMINE 2 RECEPTOR ANTAGONISTS

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Page/Page column 18-19, (2008/12/06)

The present invention relates to 6-(piperidin-4-ylamino)pyridazin-3-carbonitriles of formula (I) that are fast dissociating dopamine 2 receptor antagonists, processes for preparing these compounds, pharmaceutical compositions comprising these compounds as an active ingredient. The compounds find utility as medicines for treating or preventing central nervous system disorders, for example schizophrenia, by exerting an antipsychotic effect without motor side effects.

Discovery of potent, selective, orally bioavailable stearoyl-CoA desaturase 1 inhibitors

Liu, Gang,Lynch, John K.,Freeman, Jennifer,Liu, Bo,Xin, Zhili,Zhao, Hongyu,Serby, Michael D.,Kym, Philip R.,Suhar, Tom S.,Smith, Harriet T.,Cao, Ning,Yang, Ruojing,Janis, Rich S.,Krauser, Joel A.,Cepa, Steven P.,Beno, David W. A.,Sham, Hing L.,Collins, Christine A.,Surowy, Teresa K.,Camp, Heidi S.

, p. 3086 - 3100 (2008/02/10)

Stearoyl-CoA desaturase 1 (SCD1) catalyzes the committed step in the biosynthesis of monounsaturated fatty acids from saturated, long-chain fatty acids. Studies with SCD1 knockout mice have established that these animals are lean and protected from leptin

Aromatic compounds and pharmaceutical compositions containing them

-

, (2008/06/13)

The invention relates to compounds of formula I and pharmaceutically acceptable salts and in vivo hydrolysable esters and amides thereof and processes for their preparation, their use as therapeutic agents and pharmaceutical compositions containing them.

Fungicidal pyridazines

-

, (2008/06/13)

Plants are protected from the damaging effects of Phycomycetous fungi by a series of pyridazines of formula STR1 wherein R3 is chloro, bromo, methyl, cyano or iodo; R is chloro, bromo, iodo, methyl, cyano or furan-2-ylmethoxy; R1 is

Synthesis and antihypertensive activity of novel 6-substituted-3-pyridazinylhydrazones

Szilagyi,Kasztreiner,Matyus,et al.

, p. 111 - 117 (2007/10/02)

The synthesis and hypotensive properties of a series of 6-substituted-3-pyridazinylhydrazones are described. The most active compound of the series. 1-(6-morpholino-3-pyridazinyl)-2-[1-(tert-butoxycarbonyl)-2-propylidene] hydrazine, is a more potent hypotensive agent than hydralazine with a longer duration of action and a lower toxicity. Structure-activity relationships are discussed.

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