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1,4-Dimorpholino-1,2,3,4-tetrathiabutane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16131-53-6

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16131-53-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16131-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,3 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16131-53:
(7*1)+(6*6)+(5*1)+(4*3)+(3*1)+(2*5)+(1*3)=76
76 % 10 = 6
So 16131-53-6 is a valid CAS Registry Number.

16131-53-6SDS

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 4,4'-Tetrathiobismorpholine

1.2 Other means of identification

Product number -
Other names -

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:16131-53-6 SDS

16131-53-6Downstream Products

16131-53-6Relevant academic research and scientific papers

Crystal and Molecular Structures of Dimorpholinotetrasulphane

Foss, Olav,Janickis, Vitalijus

, p. 632 - 633 (1980)

The tetrasulphane S4(NC4H8O)2 crystallizes in the tetragonal space group I41/a (no. 88) with a=b=12.812(1), c=16.733(2) Angstroem, and Z=8.The structure has been determined by X-ray diffraction from Mo-Kα diffractometer data and refined by full-matrix least-squares to R 0.045 for 948 observed reflections.The molecules lie across crystallographic two-fold axes.The N-S-S-S-S-N chains occur in the trans-trans form, with N-S 1.668(3), S-S (terminal) 2.061(2), S-S (central) 2.078(3) Angstroem, N-S-S 109.1(2), S-S-S 105.8(1) deg, NSS-SSS 90.3. and SSS-SSS 79.9 deg.The morpholine groups occur in the chair form, with N-S equatorial.The S-S bonds alternate only slightly in length along the chain, like the Se-Se bonds in the isomorphous tetraselane analogue.

INTERACTION OF THIOUREA WITH SULFUR DIVALENT COMPOUNDS: DESULFURIZATION OF THIOUREA BY N,N'-THIOBISMORPHOLINE

Diaz, C.,Bustos, O.,Yutronic, N.

, p. 207 - 214 (2007/10/02)

The reaction of thiourea with several sulfur(II)-nitrogen compounds as well as thioethers and thiophenol have been investigated.At room temperature reaction of thiourea with N,N'-dithiobisamines afford compounds of composition H2N-C(S)-NH-S-S-NR2 while at high temperature sulfur and a complex mixture of S-N compounds are formed.N,N'-thiobismorpholine undergoes sulfuration with thiourea, to give N,N'-tetrathiomorpholine while from the reaction of N,N'-thiobis(piperidine) with thiourea the compound was identified.From the reaction of thiourea with sulfenamides, dithioethers and thiophenol the unaltered reactives were isolated.Key words: Thiourea reactions; thiobisamines reactivity; sulfur divalent.

Process for the preparation of N-tetrathiodimorpholine

-

, (2008/06/13)

There is disclosed a process for the preparation of N-tetrathiodimorpholine wherein an admixture of morpholine and elemental sulfur is oxidized with air or oxygen in the presence of iron salts and iron complexes to yield N-tetrathiodimorpholine.

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