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Carbamic acid, [2-[[(3-methoxyphenyl)methyl]thio]ethyl](2-phenylethyl)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112393-86-9

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112393-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112393-86-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,3,9 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112393-86:
(8*1)+(7*1)+(6*2)+(5*3)+(4*9)+(3*3)+(2*8)+(1*6)=109
109 % 10 = 9
So 112393-86-9 is a valid CAS Registry Number.

112393-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name <2-<<(3-methoxyphenyl)methyl>thio>ethyl><2-phenylethyl>carbamic acid methyl ester

1.2 Other means of identification

Product number -
Other names (2-{[(3-methoxyphenyl)methyl]thio}ethyl)(2-phenylethyl)carbamic acid methyl 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:112393-86-9 SDS

112393-86-9Relevant academic research and scientific papers

Inhibition of 5-lipoxygenase by substituted 3,4-dihydro-2H-1,4-thiazines

Weintraub,Skoog,Nichols,Wiseman,Huber,Baugh,Farrell

, p. 937 - 943 (2007/10/02)

A series of substituted 3,4-dihydro-2H-1,4-thiazines inhibit 5-lipoxygenase from rat leukocytes and exhibit submicromolar IC50 values. A novel synthesis of these compounds was developed based on the formation of hydroxymethyleneamine 13 and its

HETEROCYCLES. 11. SULFUR ANALOGS OF 3-(3-HYDROXYPHENYL)-N-n-PROPYLPIPERIDINE

Weintraub, Philip M.,Miller, Frank P.,Wiech, Norbert L.

, p. 1503 - 1516 (2007/10/02)

Analogs of 3-(3-hydroxyphenyl)-N-n-propylpiperidine (3-PPP) and 3-(3-hydroxyphenyl)-N-(2-phenylethyl)piperidine (phenethyl 3-PP) in which carbon 4 was replaced by sulfur were synthesized and tested for dopamine autoreceptor activity.

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