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1,3-Benzodioxol-5-yl(morpholin-4-yl)methanethione is a complex organic compound with the molecular formula C12H14N2O3S. It is characterized by a benzodioxole ring, which is a benzene ring with two oxygen atoms forming a dioxolane ring fused to it, and a morpholine ring, which is a cyclic amine with a four-membered ring. The compound features a methylenethione group (-CH2-S-) connecting the benzodioxole and morpholine moieties. This chemical is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as a building block for the development of new compounds with biological activity. Its structure provides a unique combination of aromatic, heterocyclic, and sulfur-containing functional groups, which can contribute to its reactivity and potential therapeutic properties.

7501-62-4

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7501-62-4 Usage

Chemical compound

Yes

Physical state

Colorless to pale yellow liquid

Odor

Sweet, floral

Usage

Precursor in the synthesis of MDMA (ecstasy)

Family classification

Phenylpropene

Natural occurrence

Found in essential oils of sassafras and certain other plants

Regulation

Use and production are heavily regulated due to potential for abuse and toxic properties

Health risks

Ingestion or inhalation can be harmful, causing liver damage and carcinogenicity

Control status

Highly controlled substance in many countries

Check Digit Verification of cas no

The CAS Registry Mumber 7501-62-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7501-62:
(6*7)+(5*5)+(4*0)+(3*1)+(2*6)+(1*2)=84
84 % 10 = 4
So 7501-62-4 is a valid CAS Registry Number.

7501-62-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-benzodioxol-5-yl(morpholin-4-yl)methanethione

1.2 Other means of identification

Product number -
Other names Benzo[1,3]dioxol-5-yl-morpholin-4-yl-methanethione

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:7501-62-4 SDS

7501-62-4Relevant academic research and scientific papers

A simple and direct method for converting thioamides into thioesters

Harrowven, David C.,Lucas, Matthew C.,Howes, Peter D.

, p. 1187 - 1196 (2007/10/03)

Thioamides may be transformed into thioesters through the simple expedient of warming them in an aqueous THF solution containing an alkylating agent. Reactions proceed in high yield and are amenable to multi-gram scale.

Infrared spectra of several thiopiperidides and thiomorpholides

Cornea, Felicia,Cercasov, Cornelia,Ciureanu, Mariana

, p. 775 - 782 (2007/10/02)

Infrared spectra in the 1700-500 cm-1 region have been studied for several types of thiopiperidides (thiobenzoylpiperidides, thiocinnamoylpiperidides and phenylthioacetpiperidides) and for the corresponding thiomorpholides.Three characteristic thioamide bands were located and assigned.The behaviour of these bands on molecular complexing (with iodine as an electron acceptor) was used to support the assignments.The experimental data were discussed in terms of the theoretical results obtained by an HMO procedure.

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