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N-(3-CHLOROPYRIDAZIN-6-YL)-N-METHYLHYDRAZINE, a hydrazine derivative with the molecular formula C5H7ClN4, features a chlorine-substituted pyridazine ring. This chemical compound is utilized as a building block in the synthesis of various biologically active molecules and compounds, particularly in the pharmaceutical and agrochemical industries.

76953-33-8

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76953-33-8 Usage

Uses

Used in Pharmaceutical Industry:
N-(3-CHLOROPYRIDAZIN-6-YL)-N-METHYLHYDRAZINE is used as a synthetic intermediate for the development of biologically active molecules and compounds. Its antitumor and antimicrobial properties make it a valuable component in the creation of pharmaceuticals for medical applications.
Used in Agrochemical Industry:
In the agrochemical sector, N-(3-CHLOROPYRIDAZIN-6-YL)-N-METHYLHYDRAZINE is employed as a precursor in the synthesis of agrochemicals. Its antimicrobial properties contribute to the development of products that can protect crops from diseases and pests, thereby enhancing agricultural productivity.
It is crucial to handle and use N-(3-CHLOROPYRIDAZIN-6-YL)-N-METHYLHYDRAZINE with care due to its potential hazards and toxicity. Proper safety measures should be implemented to minimize risks during its application in both the pharmaceutical and agrochemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 76953-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,5 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76953-33:
(7*7)+(6*6)+(5*9)+(4*5)+(3*3)+(2*3)+(1*3)=168
168 % 10 = 8
So 76953-33-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H7ClN4/c1-10(7)5-3-2-4(6)8-9-5/h2-3H,7H2,1H3

76953-33-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6-chloropyridazin-3-yl)-1-methylhydrazine

1.2 Other means of identification

Product number -
Other names OR4821

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:76953-33-8 SDS

76953-33-8Relevant academic research and scientific papers

STRUCTURE OF 3-CHLORO-6-HYDRAZINOPYRIDAZINE IN SOLUTIONS

Buzykin, B. I.,Maksimova, A. A.,Stolyarov, A. P.,Flegontov, S. A.,Kitaev, Ju. P.

, p. 1193 - 1196 (1982)

It is shown by means of the fixed-structure method, UV spectroscopy and dipole-moment method that the product of the reaction of 3,6-dichloropyridazine with hydrazine in solution in methanol and acetonitrile has the 3-chloro-6-hydrazinopyridazine structur

INHIBITORS OF FLAVIVIRIDAE VIRUSES

-

Page/Page column 54, (2011/08/04)

Provided are compounds of Formula I: and pharmaceutically acceptable salts and esters thereof. The compounds, compositions, and methods provided are useful for the treatment of Flaviviridae virus infections, particularly hepatitis C infections.

N-PHENYL-1,1,1-TRIFLUOROMETHANESULFONAMIDE HYDRAZONE DERIVATIVE COMPOUNDS AND THEIR USAGE IN CONTROLLING PARASITES

-

Page/Page column 38, (2008/06/13)

Novel N-phenyl-1,1,1-trifluoromethanesulfonamide compounds useful for controlling endo and/or ectoparasites in the environment are provided, together with methods of making the same, and methods of using the inventive compounds to treat parasite infestations in vivo and ex vivo.

Nucleophilic substitution of chlorine with hydrazine and methylhydrazine in chlorinated pyridazines and pyridazones

Baranov,Tsypin,Malin,Laskin

, p. 1997 - 2000 (2007/10/03)

The reactions of methylhydrazine and hydrazine hydrate with chlorinated pyridazines and pyridazones were studied.

Process for preparing N-pyrrolyl-pyridazineamine derivatives

-

, (2008/06/13)

The present invention refers to a new process for preparing N-2,3,4,5-substituted-1H-pyrrol-1-yl)-6-substituted amino-3-pyridazineamine, known as antihypertensive agents. The process is characterized in that a suitable 3,6-dihalogenopyridazine is reacted with hydrazine hydrate or other hydrazine derivatives of formula NH2 NHR, the obtained compound is reacted with a suitable dicarbonyl compound yielding first an alcandione-bis-[6-halogen-3-pyridazininyl]hydrazone, and then a 6-halogen-3-pyrrolylpyridazineamine derivative which is in turn reacted with an amine to yield the desired compounds.

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