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4,4,5,5-Tetramethyl-2-sulfanyl-1,3,2-dioxaphospholane 2-sulfide is a complex organic compound with the molecular formula C6H14O2PS3. It is a cyclic phosphorus-containing molecule, characterized by the presence of a phospholane ring, which consists of a phosphorus atom bonded to two oxygen atoms and a sulfur atom. The molecule also features two methyl groups attached to each of the carbon atoms adjacent to the phosphorus, contributing to its stability and reactivity. 4,4,5,5-tetramethyl-2-sulfanyl-1,3,2-dioxaphospholane 2-sulfide is of interest in the field of organophosphorus chemistry, potentially serving as a building block for more complex molecules or as a reagent in chemical synthesis. Its unique structure and properties may also make it a candidate for applications in materials science or as a precursor in the production of pharmaceuticals.

699-36-5

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699-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 699-36-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 699-36:
(5*6)+(4*9)+(3*9)+(2*3)+(1*6)=105
105 % 10 = 5
So 699-36-5 is a valid CAS Registry Number.

699-36-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4,5,5-tetramethyl-2-sulfanyl-2-sulfanylidene-1,3,2λ<sup>5</sup>-dioxaphospholane

1.2 Other means of identification

Product number -
Other names 1,3,2-Dioxaphospholane,2-mercapto-4,4,5,5-tetramethyl-,2-sulfide

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:699-36-5 SDS

699-36-5Relevant academic research and scientific papers

Synthesis, spectral and sol-gel behavior of mixed ligand complexes of titanium(iv) with oxygen, nitrogen and sulfur donor ligands

Srivastava, Abhishek,Srivastava, Neetu,Tripathi, Umesh Nath

, p. 61 - 76 (2021/06/03)

A new route to synthesize nano-sized Ti(IV) mixed ligand complexes have been investigated by the reaction of titanium(IV) chloride with ammonium salts of dithiophosphate and 3(2'-hydroxyphenyl)-5-(4- substituted phenyl) pyrazolines. The resultant complex is then treated with H2S gas to get sulfur bridged dimer of Ti(IV) complex, a precursor of TiS2. The morphology of the complexes was studied by employing XRD which shows that all the complexes are amorphous solid. Molecular weight measurements, elemental analysis in conjugation with spectroscopic (IR, 1H NMR, 13C NMR and 31P NMR) studies revealed the dimeric nature of the complexes in which pyrazoline and dithiophosphate are bidentate. Scanning electron microscopic image and XRD indicate that the particles are in the nano range (50 nm). Putting all the facts together, coordination number six is proposed for titanium with octahedral geometry.

Synthesis, spectral characterization and antibacterial activity of O, O’-dialkyl and alkylene dithiophosphatogold (III)dichloride; crystal structure of [S2POCMe2CMe2O]AuCl2

Elkhaldy, Adnan A. S.,Gaikwad, Dnyaneshwar,Staples, Richard J.,Janen, Afef,Boni, Yannic

, p. 871 - 876 (2019/02/05)

O, O’-Dialkyl and alkylene dithiophosphatogold (III)dichloride complexes of the type [(RO)2PS2]AuCl2 and [S2POGO]AuCl2, where R = Et, nPr, iPr, iBu, Ph, cyclohexyl and cyclopentyl, where G = CMe2CMe2-, have been synthesized in 80-90% yields by reaction of the corresponding acid or sodium salts of the appropriate dithiophosphoric acids in 1:1 ratio with gold (III) chloride in dry dichloromethane at room temperature. The compounds have been characterized by elemental analyses, IR and (1H, l3C, and 31P) NMR. The crystal structure of [S2POCMe2CMe2O]AuCl2, was determined. These new complexes have shown their growth inhibiting potential against various bacterial strains with moderate to good activity.

Synthesis of S-thioacyl dithiophosphates, efficient and chemoselective thioacylating agents

Doszczak, Leszek,Rachon, Janusz

, p. 1271 - 1279 (2007/10/03)

Easily available acyl dithiophosphates are not stable and isomerise reversibly to O-thioacyl monothiophosphates, especially when subjected to heating. Much slower but probably irreversible isomerisation to S-thioacyl monothiophosphates occurs. Since equilibrium states are established and S-thioacyl (mono)thiophosphates form slowly, reaction mixtures contain generally both thioacylating and acylating agents, and consequently cannot be used for efficient thioacylation. On the other hand, treatment of a mixture of isomeric anhydrides with an excess of a dithiophosphoric acid leads to exclusive formation of S-thioacyl dithiophosphates. They appear to be excellent thioacylating agents: relatively stable, inert towards water and oxygen and therefore easy to handle. Reactions with nitrogen or sulfur nucleophiles proceed very rapidly under ambient conditions, yielding respective thioacyl derivatives. Isolation of the products is very simple. Due to the low reactivity of S-thioacyl dithiophosphates towards oxygen nucleophiles they can be used for direct thioacylation of multifunctional nucleophiles with unprotected hydroxy groups. Respective thioacyl derivatives cannot readily be obtained using other methods.

SYNTHESIS AND CHARACTERIZATION OF 2-MERCAPTO-2-THIONO-1,3,2-DIOXAPHOSPHOLANES AND DIOXAPHOSPHORINANES

Chauhan, H. P. S.,Bhasin, C. P.,Srivastava, G.,Mehrotra, R. C.

, p. 99 - 104 (2007/10/02)

2-Mercapto-2-thiono-1,3,2-dioxaphospholanes and dioxaphosphorinanes, have been synthesized by the reactions of phosphorus pentasulfide with some 1,2-diols (viz., butane-2,3-diol and 2,3-dimethylbutane-2,3-diol) and 1,3-diols (viz., 2-methylpentane-2,4-diol, 2,2-dimethylpropane-1.3-diol and 2,2-diethylpropane-1,3-diol) in 1:2 molar ratio in dry benzene.These volatile compounds have been purified by distillation under reduced pressure.The 2-methylpentane-2,4-diol derivative, however, decomposed during attempted distillations.These new compounds have been characterized by elemental analysis, molecular weight determinations, measurement of pKa values and IR as well as NMR spectroscopic studies.The ammonium and sodium salts of some of these acids have also been characterized.

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