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10,12-Dimethyl-1,4,7-trioxa-10,12-diazacyclotetradecane-11-thione is a complex organic compound with the molecular formula C10H21N2O3S. It is a cyclic molecule containing three oxygen atoms, two nitrogen atoms, and one sulfur atom, with two methyl groups attached at the 10th and 12th positions. 10,12-Dimethyl-1,4,7-trioxa-10,12-diazacyclotetradecane-11-thione is characterized by its unique structure, which features a 14-membered ring with alternating oxygen, nitrogen, and carbon atoms, and a sulfur atom at the 11th position. It is an example of a thione, which is a sulfur analog of a thiol, and is known for its potential applications in various chemical reactions and as a building block for more complex molecules. Due to its specific structure, it may have unique chemical properties and reactivity, making it a subject of interest in organic chemistry research.

89863-08-1

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89863-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89863-08-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,6 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89863-08:
(7*8)+(6*9)+(5*8)+(4*6)+(3*3)+(2*0)+(1*8)=191
191 % 10 = 1
So 89863-08-1 is a valid CAS Registry Number.

89863-08-1SDS

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 4,6-dimethyl-1,9,12-trioxa-4,6-diazacyclotetradecane-5-thione

1.2 Other means of identification

Product number -
Other names 1,9,12-Trioxa-4,6-diazacyclotetradecane-5-thione,4,6-dimethyl

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:89863-08-1 SDS

89863-08-1Downstream Products

89863-08-1Relevant academic research and scientific papers

MACROHETEROCYCLES. XXII. N,N'-DIALKYLDIAZA(OXA)CYCLOALKANETHIONES, SYNTHESIS AND PROPERTIES

Bogat-skii, A. V.,Luk'yanenko, N. G.,Kirichenko, T. I.,Limich, V. V.,Nazarova, N. Yu.,Karpenko, L. P.

, p. 1379 - 1385 (2007/10/02)

During the alkylation of diaza(oxa)cycloalkanethiones with halogenoalkanes in a two-phase system in the presence of potassium carbonate the corresponding N,N'-dialkylthiuronium salts are formed.Heating of the latter under vacuum leads to the elimination of the halogenoalkanes and the formation of N,N'-dialkyldiaza(oxa)cycloalkanethiones, including new crown compounds.The cationic selectivity of the latter with respect to the ions of alkali and alkaline-earth metals was determined.

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