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78140-52-0

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78140-52-0 Usage

Chemical Properties

YELLOW CRYSTALLINE POWDER

Uses

3-(Isothiocyanatomethyl)-2,2,5,5-tetramethyl-1-pyrrolidinyloxy (cas# 78140-52-0) is a compound useful in organic synthesis.

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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