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Methanone, [4-(1-methylethyl)phenyl](3-methyl-5-isothiazolyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90695-86-6

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90695-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90695-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,9 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90695-86:
(7*9)+(6*0)+(5*6)+(4*9)+(3*5)+(2*8)+(1*6)=166
166 % 10 = 6
So 90695-86-6 is a valid CAS Registry Number.

90695-86-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methyl-1,2-thiazol-5-yl)-(4-propan-2-ylphenyl)methanone

1.2 Other means of identification

Product number -
Other names 4-(1-methylethyl)phenyl 3-methylisothiazol-5-yl ketone

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:90695-86-6 SDS

90695-86-6Relevant academic research and scientific papers

Heterocyclic Analogues of Chlorcyclizine with Potent Hypolipidemic Activity

Ashton, Michael J.,Ashford, Alan,Loveless, Anthony H.,Riddell, David,Salmon, John,Stevenson, Gregory V.W.

, p. 1245 - 1253 (2007/10/02)

A series of piperazines was synthesized and their effect of reducing serum cholesterol and triglyceride levels in the rat was evaluated.A systematic exploration of the structure-activity relationships led to the synthesis of (R,S)-(3,5-dimethylisoxazol-4-yl)(4-methylpiperazin-1-yl)methane dihydrochloride (M and B 31426), which had potent activity in lowering serum lipid levels at a daily oral dose of 2 mg/kg and was 100 times more potent than clofibrate.

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