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78140-52-0

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78140-52-0 Usage

Description

3-(ISOTHIOCYANATOMETHYL)-2,2,5,5-TETRAMETHYL-1-PYRROLIDINYLOXY, with the chemical abstracts service number 78140-52-0, is a synthetic compound that plays a significant role in various organic synthesis processes. Its unique molecular structure, featuring an isothiocyanatoethyl group attached to a tetramethyl-1-pyrrolidinyloxy core, endows it with versatile reactivity and potential applications across different chemical and industrial domains.

Uses

Used in Organic Synthesis:
3-(ISOTHIOCYANATOMETHYL)-2,2,5,5-TETRAMETHYL-1-PYRROLIDINYLOXY is used as a key intermediate in the synthesis of various organic compounds. Its isothiocyanate functionality allows it to react with a wide range of nucleophiles, facilitating the formation of diverse chemical products. This makes it a valuable building block for the creation of pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(ISOTHIOCYANATOMETHYL)-2,2,5,5-TETRAMETHYL-1-PYRROLIDINYLOXY is used as a precursor for the development of new drugs. Its ability to form stable conjugates with biologically active molecules can lead to the discovery of novel therapeutic agents with improved pharmacological properties, such as enhanced stability, bioavailability, and target specificity.
Used in Agrochemical Industry:
3-(ISOTHIOCYANATOMETHYL)-2,2,5,5-TETRAMETHYL-1-PYRROLIDINYLOXY also finds application in the agrochemical sector, where it serves as a starting material for the synthesis of new pesticides and herbicides. Its reactivity and structural features can be leveraged to design compounds with increased efficacy and selectivity, contributing to more sustainable agricultural practices.
Used in Specialty Chemicals:
In the specialty chemicals market, 3-(ISOTHIOCYANATOMETHYL)-2,2,5,5-TETRAMETHYL-1-PYRROLIDINYLOXY is utilized for the production of high-value compounds with specific applications. These may include materials for coatings, adhesives, and polymers, where its unique properties can impart desirable characteristics such as improved durability, resistance to environmental factors, and tailored mechanical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 78140-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,1,4 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78140-52:
(7*7)+(6*8)+(5*1)+(4*4)+(3*0)+(2*5)+(1*2)=130
130 % 10 = 0
So 78140-52-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H18N2OS/c1-9(2)5-8(6-11-7-14)10(3,4)12(9)13/h8,13H,5-6H2,1-4H3/t8-/m1/s1

78140-52-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-3-(isothiocyanatomethyl)-2,2,5,5-tetramethylpyrrolidine

1.2 Other means of identification

Product number -
Other names 2,2,5,5-tetramethyl-3-isothiocyanatomethylpyrrolidine-1-oxyl

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:78140-52-0 SDS

78140-52-0Downstream Products

78140-52-0Relevant articles and documents

Reaction of Nitroxides with Sulfur Containing Compounds II [1]. Preparation of Nitroxides Bearing an Isothiocyanate Substituent in View of the Nitroxyl Group Reduction with Thiophosgene

Zakrzewski, Jerzy,Hupko, Jarosllaw,Kryczka, Krzysztof

, p. 843 - 850 (2007/10/03)

The reaction of thiophosgene with 2,2,6,6-tetramethylpiperidine-1-oxyl (used as a model nitroxyl radical) was examined. 2,2,6,6-Tetramethylpiperidine and 2,2,6,6-tetramethyl-1-hydroxypiperidine were identified as products. The reaction is not competitive with the reaction of thiophosgene with an amino group. Thus, three nitroxides with an isothiocyanate group were synthesized from thiophosgene and the nitroxides containing the amino substituent.

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