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1,9,12-TRIOXA-4,6-DIAZACYCLOTE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75491-64-4

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75491-64-4 Usage

Structure

Cyclic ether with a six-membered ring containing alternating oxygen and nitrogen atoms

Usage

Precursor in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals

Industry applications

Wide range of applications in the chemical industry due to its unique structure and reactivity

Chelating agent

Potential as a chelating agent for binding and removing heavy metals from the environment

Research interest

Versatile properties and potential uses in various fields attract attention from researchers and chemists

Check Digit Verification of cas no

The CAS Registry Mumber 75491-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,9 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75491-64:
(7*7)+(6*5)+(5*4)+(4*9)+(3*1)+(2*6)+(1*4)=154
154 % 10 = 4
So 75491-64-4 is a valid CAS Registry Number.

75491-64-4SDS

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

1.2 Other means of identification

Product number -
Other names HMS2281M09

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:75491-64-4 SDS

75491-64-4Relevant academic research and scientific papers

Macroheterocycles. III. Synthesis, properties, and tautomeric transformations of macrocyclic thioureas

Bogatskii, A.V.,Luk'yanenko, N. G.,Kirichenko, T. I.

, p. 1124 - 1129 (2007/10/02)

Macrocyclic thioureas of the and types, where R=CH2(CH2OCH2)nCH2 and (CH2)m (n=1, 2, 3, m=8), were obtained for the first time by the reaction of diamines with carbon bisulfide.The UV, IR, and PMR spectra of the compounds were studied.It was shown that they exist in the thione form in the crystalline state and in protic solvents.Thione - thiol isomerization is observed in nonpolar solvents.

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