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1007-55-2

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1007-55-2 Usage

General Description

6-chloro-N-(propan-2-yl)pyridazin-3-amine is a chemical compound with a molecular formula of C7H10ClN3. This substance falls under the category of organic compounds known as pyridazines and pyridazine derivatives. These are compounds containing a pyridazine ring, which is a six-membered aromatic ring with two nitrogen atoms at positions 1 and 2, and four carbon atoms. The specific features of 6-chloro-N-(propan-2-yl)pyridazin-3-amine include a propan-2-yl group attached to the nitrogen atom and a chlorine atom attached to the 6th carbon of the pyridazine ring. Further information about its properties, including its physical and chemical properties, toxicological data, or usage, isn't broadly documented in scientific literature.

Check Digit Verification of cas no

The CAS Registry Mumber 1007-55-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1007-55:
(6*1)+(5*0)+(4*0)+(3*7)+(2*5)+(1*5)=42
42 % 10 = 2
So 1007-55-2 is a valid CAS Registry Number.

1007-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-N-propan-2-ylpyridazin-3-amine

1.2 Other means of identification

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

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:1007-55-2 SDS

1007-55-2Upstream product

1007-55-2Downstream Products

1007-55-2Relevant articles and documents

Quinoxaline studies. 23. Potential antimalarials. Substituted 5,8-dimethoxy-6-[N-(omega-dimethylaminoalkyl)amino]quinoxalines were prepared: the first series with identical 2,3-substituents H, CH3, C6H5, C6H4-4-Cl, and CH2C6H5; and the second with identical styryl groups CH=CHC6H5, CH=CHC6H4-4-Cl, CH=CHC6H3-3,4-Cl2, CH=CHC6H4-4-F, CH=CHC6H4-4-CF3, and CH=CHC6H4-4-NO2. None of the substances

Pifferi,Parravicini,Carpi,Dorigotti

, p. 741 - 746 (2007/10/04)

3-Hydrazinopyridazines substituted in position 6 with a primary amine, secondary amine, or an alkoxy group were synthesized and screened for antihypertensive activity. In general, the 6-dialklamino derivatives are the most active; the (2-hydroxypropyl)methylamino chain provides the best combination of high antihypertensive activity and toxicity.

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