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ethyl 5-amino-1-(6-hydrazinopyridazin-3-yl)-1H-pyrazole-4-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69720-59-8

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69720-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69720-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,2 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69720-59:
(7*6)+(6*9)+(5*7)+(4*2)+(3*0)+(2*5)+(1*9)=158
158 % 10 = 8
So 69720-59-8 is a valid CAS Registry Number.

69720-59-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-amino-1-(6-hydrazinylpyridazin-3-yl)pyrazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names 5-Amino-1-(6-hydrazino-3-pyridazinyl)-1H-pyrazole-4-carboxylic acid ethyl ester

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:69720-59-8 SDS

69720-59-8Upstream product

69720-59-8Downstream Products

69720-59-8Relevant academic research and scientific papers

3-(1-Pyrazolyl)-pyridazine derivatives

-

, (2008/06/13)

3-(1-Pyrazolyl)-pyridazine derivatives of the formula I, or pharmaceutically acceptable acid addition salts thereof, which decrease high blood pressure and inhibit catabolism or prostaglandins, STR1 wherein R1 is hydrogen or C1-4 alkyl, R2 is hydrogen, cyano, carboxyl, carbamoyl, carbaxoyl or C1-4 alkoxycarbonyl, R3 is hydrogen or chlorine or --NR4 NHR5 or NR6 R7, wherein R4 and R5 are each hydrogen or C1-4 alkyl, wherein R6 and R7 are each hydrogen or C1-5 alkyl, C1-5 hydroxyalkyl, C3-7 cycloalkyl, phenyl or benzyl, or benzyl or phenylethyl substituted with one or two chlorine atoms or methoxy groups, or a furylmethyl, pyridylmethyl, pyrrolidine or piperazine ring, or when R7 is hydrogen, R6 is --(CH2)n --NR4 R5 wherein n is an integer from 1 to 3.

Studies in the field of pyridazine compounds, III (1). Hypotensive 3-(1-pyrazolyl) pyridazine derivatives

Szilagyi,Kasztreiner,Tardos,et al.

, p. 439 - 445 (2007/10/05)

Substituted 3-(1-pyrazolyl)pyridazines were synthesized and their hypotensive activity was evaluated on anaesthetized normotensive cats and awake spontaneously hypertensive rats. Several relations were found between structure and hypotensive activity of the compounds. Some of the active compounds proved to be useful for detailed investigations. Most of the active compounds exerted an influence on prostaglandin metabolism.

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