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METHYL L-2-ISOTHIOCYANATO-3-PHENYLPROPIONATE, also known as MEP, is a chemical compound that is commonly used in the production of fragrances and flavorings. It is known for its antimicrobial and insecticidal properties, making it a potential candidate for the development of pest control and preservation products. Additionally, MEP is being researched for its potential pharmacological applications, particularly in the area of cancer treatment. However, further studies are needed to fully understand its effects and potential benefits in these areas. Overall, MEP is a versatile and valuable chemical compound with a range of potential uses in various industries.

68521-58-4

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68521-58-4 Usage

Uses

Used in Fragrance and Flavoring Industry:
METHYL L-2-ISOTHIOCYANATO-3-PHENYLPROPIONATE is used as a key ingredient in the manufacture of fragrances and flavorings due to its unique chemical properties.
Used in Pest Control and Preservation Products:
METHYL L-2-ISOTHIOCYANATO-3-PHENYLPROPIONATE is used as an active ingredient in pest control and preservation products due to its antimicrobial and insecticidal properties.
Used in Cancer Treatment Research:
METHYL L-2-ISOTHIOCYANATO-3-PHENYLPROPIONATE is used as a subject of research in the field of cancer treatment, with the aim of understanding its potential pharmacological applications and benefits.
Used in Drug Development:
METHYL L-2-ISOTHIOCYANATO-3-PHENYLPROPIONATE is used as a potential candidate for the development of new drugs, particularly in the area of cancer treatment, as it is being researched for its potential pharmacological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 68521-58-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,5,2 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 68521-58:
(7*6)+(6*8)+(5*5)+(4*2)+(3*1)+(2*5)+(1*8)=144
144 % 10 = 4
So 68521-58-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO2S/c1-14-11(13)10(12-8-15)7-9-5-3-2-4-6-9/h2-6,10H,7H2,1H3/t10-/m0/s1

68521-58-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl L-2-isothiocyanato-3-phenylpropionate

1.2 Other means of identification

Product number -
Other names METHYL L-2-ISOTHIOCYANATO-3-PHENYLPROPIONATE

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:68521-58-4 SDS

68521-58-4Downstream Products

68521-58-4Relevant academic research and scientific papers

Utilization of methyl 3-Aryl-2-thiocyanatopropanoates in the synthesis of 2-(4-morpholinyl)- and 2-(piperazinyl)-5-(benzyl)thiazol-4-ones1

Obushak, Mykola D.,Karpyak, Volodymyr V.,Ostapiuk, Yuri V.,Matiychuk, Vasyl S.

, p. 1437 - 1445 (2008/02/08)

By the reaction of methyl acrylate with arenediazonium salts and KSCN in the presence of copper(II) acetate, the methyl 3-aryl-2-thiocyanatopropanoates 2 have been obtained. These compounds react with morpholine or monosubstituted piperazines in the prese

IODOARYLATION OF ACRYLONITRILE AND ACRYLIC ESTERS WITH ARENEDIAZONIUM SALTS

Ganushchak, N. I.,Obushak, N. D.,Polishchuk, O. P.

, p. 2291 - 2295 (2007/10/02)

In the reaction of acrylic esters and acrylonitrile with arenediazonium salts in the presence of alkali-metal iodides the products from addition of the aryl radical and iodine at the double bond are formed.An effective method is proposed for the synthesis of 1-iodo-1-methoxycarbonyl(cyano)-2-arylalkanes, which enter readily into nucleophilic substitution of iodine.When boiled with an alcohol solution of alkali, they are transformed into derivatives of cinnamic acid.

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