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"7-[(4-methylpiperazin-1-yl)methyl]-5-[(phenylsulfanyl)methyl]quinolin-8-ol" is a complex organic compound characterized by a quinolin-8-ol core structure, which features a hydroxyl group at the 8th position. The molecule is further defined by a 4-methylpiperazin-1-ylmethyl group attached at the 7th position, contributing to its nitrogen-containing ring structure, and a phenylsulfanylmethyl group at the 5th position, which introduces a sulfur atom bonded to a benzene ring. 7-[(4-methylpiperazin-1-yl)methyl]-5-[(phenylsulfanyl)methyl]quinolin-8-ol is likely to be of interest in medicinal chemistry due to its potential pharmacological properties, given the presence of multiple functional groups that can interact with biological targets.

6064-31-9

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6064-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6064-31-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6064-31:
(6*6)+(5*0)+(4*6)+(3*4)+(2*3)+(1*1)=79
79 % 10 = 9
So 6064-31-9 is a valid CAS Registry Number.

6064-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dimethyl-4-Undecanone

1.2 Other means of identification

Product number -
Other names -

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

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More Details:6064-31-9 SDS

6064-31-9Downstream Products

6064-31-9Relevant academic research and scientific papers

NOVEL SYNTHESIS OF INTERNAL ALKENYLDIALKYLBORANE BY THE REACTION OF 1-HALO-1-ALKENYLDIALKYLBORANE WITH GRIGNARD REAGENT.

Arase,Hoshi,Masuda

, p. 209 - 213 (2007/10/02)

To synthesize internal alkenyldialkylboranes, coupling reactions were carried out by using 1-halo-1-alkenyldialkylboranes and Grignard reagents. Hydrogen peroxide oxidation and protonolysis with acetic acid of the reaction product revealed that internal (E)-alkenyldialkylborane was formed in 60-90% yield.

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