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15980-15-1

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15980-15-1 Usage

Chemical Properties

clear colorless to yellow liquid

Uses

Different sources of media describe the Uses of 15980-15-1 differently. You can refer to the following data:
1. 1,4-Oxathiane is a useful reactant and reagent for organic reactions. It has been used as an oxygen donor adduct to study the growth of ZnO nanowires through chemical vapour deposition.
2. 1,4-Thioxane (1,4-oxathiane) was used to study the growth and characterization of the vertically aligned zinc oxide (ZnO) nanowires.

Safety Profile

Moderately toxic by ingestion. Mildly toxic by inhalation. A skin and eye irritant. Flammable liquid when exposed to heat, sparks,flame, or oxidizers. Forms explosive complexes with silver perchlorate or copper(I) perchlorate. Incompatible with metal perc

Check Digit Verification of cas no

The CAS Registry Mumber 15980-15-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,8 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15980-15:
(7*1)+(6*5)+(5*9)+(4*8)+(3*0)+(2*1)+(1*5)=121
121 % 10 = 1
So 15980-15-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H8OS/c1-3-6-4-2-5-1/h1-4H2

15980-15-1 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (A18052)  1,4-Oxathiane, 98+%   

  • 15980-15-1

  • 5g

  • 326.0CNY

  • Detail
  • Alfa Aesar

  • (A18052)  1,4-Oxathiane, 98+%   

  • 15980-15-1

  • 25g

  • 894.0CNY

  • Detail
  • Aldrich

  • (131970)  1,4-Thioxane  98%

  • 15980-15-1

  • 131970-25G

  • 1,092.78CNY

  • Detail

15980-15-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-Thioxane

1.2 Other means of identification

Product number -
Other names 1,4-Oxathiane

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:15980-15-1 SDS

15980-15-1Relevant articles and documents

Reactions of bielectrophiles (ClCH2CH2)2Y with sulfur in basic reducing systems

Korchevin,Russavskaya,Alekminskaya,Deryagina

, p. 240 - 243 (2002)

A simple procedure was developed for preparing bis(β-mercaptoethyl) ether and bis(β-mecraptoethyl) sulfide from commercially available chemicals: elemental sulfur, alkali, and bis(β-chloroethyl) ether or sulfide, based on thiylation with elemental sulfur of these substrates in the aqueous system hydrazine hydrate-alkali, with initial formation of the corresponding polysulfide polymers (thiokols). Their reduction with the system hydrazine hydrate-alkali, followed by acidification of dithiolate anions, yields the corresponding dithiols. Thiokols based on bis(β-chloroethyl) ether are soluble in organic solvents; they were studied by 1H NMR.

-

Georgieff,Dupre

, p. 1104,1107 (1959)

-

Destruction of chemical warfare agent simulants by air and moisture stable metal NHC complexes

Weetman, Catherine,Notman, Stuart,Arnold, Polly L.

supporting information, p. 2568 - 2574 (2018/02/28)

The cooperative effect of both NHC and metal centre has been found to destroy chemical warfare agent (CWA) simulants. Choice of both the metal and NHC is key to these transformations as simple, monodentate N-heterocyclic carbenes in combination with silver or vanadium can promote stoichiometric destruction, whilst bidentate, aryloxide-tethered NHC complexes of silver and alkali metals promote breakdown under mild heating. Iron-NHC complexes generated in situ are competent catalysts for the destruction of each of the three targetted CWA simulants.

Synthesis of cyclic ethers from diols in the presence of copper catalysts

Bayguzina,Gimaletdinova,Khusnutdinov

, p. 1840 - 1843 (2018/02/06)

A number of cyclic ethers, namely tetrahydrofuran, 2,5-dimethyltetrahydrofuran, tetrahydropyran, 1,4-dioxane, oxepane, oxocane, and 1,4-oxathiane, have been synthesized in high yields by intramolecular dehydration of diols in the presence of copper-based catalysts.

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