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1075-68-9

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1075-68-9 Usage

General Description

4-Pyridazinamine, 3,6-dimethoxy- is a chemical compound with the molecular formula C8H10N2O2. It is a white to off-white crystalline powder with a molecular weight of 166.18 g/mol. 4-Pyridazinamine, 3,6-dimethoxy- is used in the synthesis of pharmaceuticals and agrochemicals. Its properties and reactivity make it useful in a variety of chemical reactions, and it is also used as a building block in the production of other compounds. Additionally, it is known to have potential biological activity, making it a compound of interest for further research and development in the pharmaceutical and agricultural industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1075-68-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1075-68:
(6*1)+(5*0)+(4*7)+(3*5)+(2*6)+(1*8)=69
69 % 10 = 9
So 1075-68-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H9N3O2/c1-10-5-3-4(7)6(11-2)9-8-5/h3H,1-2H3,(H2,7,8)

1075-68-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-dimethoxypyridazin-4-amine

1.2 Other means of identification

Product number -
Other names 4-amino-2,6-dimethoxypyridazine

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:1075-68-9 SDS

1075-68-9Downstream Products

1075-68-9Relevant articles and documents

A new route to aminodiazines via metalation reaction. Synthesis of an aza analogue of Nevirapine: Diazines XV

Plé, Nelly,Turck, Alain,Couture, Karine,Quéguiner, Guy

, p. 838 - 842 (2007/10/03)

A new route to aminodiazines is reported, the ortho-directed lithiation of diazines is used, followed by reaction with tosyl azide as an electrophile. The reduction of the azido or tetrazolo compounds obtained was achieved and led to the expected amines. This methodology has allowed the synthesis of new aminodiazines and an improvement in the yield of various aminodiazines previously described. This reaction was used for the preparation of an aza analogue of Nevirapine.

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