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1,4,3,5-Oxathiadiazine, 2-(4-chlorophenyl)-6-(trichloromethyl)-, 4,4-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58010-41-6

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58010-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58010-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,1 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58010-41:
(7*5)+(6*8)+(5*0)+(4*1)+(3*0)+(2*4)+(1*1)=96
96 % 10 = 6
So 58010-41-6 is a valid CAS Registry Number.

58010-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-trichloromethyl-6-(4-chlorophenyl)-1,4,3,5-oxathiadiazine-4,4-dioxide

1.2 Other means of identification

Product number -
Other names 2-(4-chloro-phenyl)-6-trichloromethyl-[1,4,3,5]oxathiadiazine 4,4-dioxide

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:58010-41-6 SDS

58010-41-6Downstream Products

58010-41-6Relevant academic research and scientific papers

Replacement of imine fragment in the ring of 2,6-disubstituted 1,4,3,5-octathiadiazine-4,4-dioxides in reaction with cyano-containing compounds

Utkina,Michurin,Shishulina

, p. 889 - 894 (2007/10/03)

Reactions of 2,6-disubstituted 1,4,3,5-octathiadiazine-4,4-dioxides with cyano-containing compounds (nitriles, thiocyanates, N,N-disubstituted cyanamides) proceeding with replacement of imine fragment in dioxide by corresponding fragment of cyanide were investigated. The limits of the reaction were revealed determined by electronic effects of substituents R1 and R2 in dioxide and R3 in cyanide. Transimination occurred in dioxides with strong electron-withdrawing substituents R 1 (CCl3, CBr3, C6F5)and weak acceptor or donor substituents R2 (4-NO2C 6H4, 4-ClC6H4, CH3) under the action of compounds R3C≡N with cyano groups of relatively high nucleophilicity (R3 = 4-ClC6H 4, C6H5, (CH3)2CHS, piperidino, morpholino, diethylamino), on the one hand, and with strong electron-withdrawing substituents R3 (CCl3) on the other hand.

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