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Phenol, 2-[(6-chloro-3-pyridazinyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106153-67-7

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106153-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106153-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,1,5 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106153-67:
(8*1)+(7*0)+(6*6)+(5*1)+(4*5)+(3*3)+(2*6)+(1*7)=97
97 % 10 = 7
So 106153-67-7 is a valid CAS Registry Number.

106153-67-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(6-chloropyridazin-3-yl)oxyphenol

1.2 Other means of identification

Product number -
Other names 6-chloropyridazin-3-yl-2-hydroxyphenyl ether

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:106153-67-7 SDS

106153-67-7Relevant academic research and scientific papers

Synthesis of alkyl or aryl pyridazinyl ethers

Chung, Hyun-A.,Kim, Jeum-Jong,Kim, Ho-Kyun,Kweon, Deok-Heon,Cho, Su-Dong,Lee, Sang-Gyeong,Yoon, Yong-Jin

, p. 639 - 646 (2005)

This paper presents the synthesis of some alkyl or aryl pyridazinyl ethers from 2-alkyl-4-halo-5-hydroxy-and 2-alkyl-4,5-dichloropyridazin-3(2H)-ones or 3,6-dichloropyridazine. Reaction of 2-alkyl-4-halo-5-hydroxypyridazin-3(2H)-ones 1 with 1,2-dibromoeth

Studies on agents with vasodilator and β-blocking activities. I

Seki,Takezaki,Ohuchi,Ohuyabu,Ishimori,Yasuda

, p. 1609 - 1616 (2007/10/02)

A series of hydrazinopyridazine derivatives combined with a β-blocking side chain were synthesized. When they were given intravenously to anesthetized rats, some of them exhibited both hypotensive and β-blocking activities. Their structure-activity relati

Pyridazinyloxy (or thio) phenyl phosphates

-

, (2008/06/13)

Organic phosphates of the formula: STR1 wherein R1 and R2 are respectively an alkyl group; R3 is a phenyl group which is substituted at least by a pyridazinyloxy or pyridazinylthio group in which the pyridazinyl group may be substituted; and X is an oxygen or sulfur atom, or a salt thereof, have marked insecticidal-acaricidal activity against plant pests and mites, household pests, with very low toxicity to warm-blooded animals and fish.

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