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5452-58-4

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5452-58-4 Usage

Chemical structure

1-morpholin-4-yl-2-tetralin-2-yl-ethanethione consists of a thiol group (-SH), a morpholine ring, and a tetralin ring.

Classification

It is a thiol compound, which means it contains a sulfhydryl group (-SH).

Strong odor

Thiol compounds are known for their strong and characteristic odor.

Potential applications

The presence of morpholine and tetralin rings suggests that the compound may have pharmaceutical or industrial applications.

Biological activity

The structural features (morpholine and tetralin rings) are commonly found in biologically active molecules and materials.

Further research needed

The specific properties and uses of this compound would require additional scientific research and testing to be determined.

Check Digit Verification of cas no

The CAS Registry Mumber 5452-58-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5452-58:
(6*5)+(5*4)+(4*5)+(3*2)+(2*5)+(1*8)=94
94 % 10 = 4
So 5452-58-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H21NOS/c19-16(17-7-9-18-10-8-17)12-13-5-6-14-3-1-2-4-15(14)11-13/h5-6,11H,1-4,7-10,12H2

5452-58-4SDS

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 1-morpholin-4-yl-2-(5,6,7,8-tetrahydronaphthalen-2-yl)ethanethione

1.2 Other means of identification

Product number -
Other names 4-[(5,6,7,8-tetrahydro-[2]naphthyl)-thioacetyl]-morpholine

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:5452-58-4 SDS

5452-58-4Relevant articles and documents

Willgerodt-kindler's microwave-enhanced synthesis of thioamide derivatives

Poupaert, Jacques H.,Duarte, Sandro,Colacino, Evelina,Depreux, Patrick,McCurdy, Christopher R.,Lambert, Didier L.

, p. 1959 - 1973 (2007/10/03)

The Willgerodt-Kindler reaction was applied to a series of aromatic aldehydes and ketones. The reactions were performed in a dipolar aprotic solvent (mainly DMF) in the presence of a base catalyst (4-methylmorpholine) and utilized microwave (mw) irradiation. The pulsed mw technique rather than the continuous irradiation was preferred because it limited side reactions and hydrogen sulfide production. While not always superior to the thermal activation of the reaction, the procedure involving repetitive short pulses of microwave irradiation was found to be faster and result in consistently cleaner products. The technique can be easily applied in a fast parallel synthesis process.

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