1,3,2, dioxathiane 2,2-dioxide, cas No.: 1073-05-8

Short description:

Chemical nomen:Trimethylene sulfate
CAS non.:1073-05-8
Molecular formula:C3h6 o4 s
Molecular pondus:138,144
HS Code.:2934999090
Europae Community (EC) Number:214-022-5
NSC numero:DXXVI) DXCV
UNII:U6r4i8lvef
Dsstox substantia ID:DTXSID4061460
Nikkaji Number:J50.789J, J3.263.010C
Wikidata:Q27290765
Mol file:1073-05-8.mol

Product Detail

Product Tags

1,3,2, dioxathiane 2,2-dioxide 1073-05-8

Synonyma: 1073-05-8; trimethylene sulfate; 1,3,2-dioxathiane 2,2-dioxide; 1,3,2, dioxathiane, 2,2, Dione; 1,3-propylene sulfate, 1,3, propaxathiane cyclic sulfate; 1,3-, dioxathian 2,2, dioxide, 1,3, propavanol, cyclic sulfate; NSC (DXXVI) DXCV, Einecs 214-022-5; U6R4I8LVE, U6R4I8LVE, Brn (DCCLXXIV) DCCLXXV, 1,3,2, dioxathiane2,2, dioxide; c3h6o4s; 1,3, propavatol, cyclic Sulphate [1,3,2] dioxathiane 2,2-dioxide; nsc526595, NSC-(DXXVI) DXCV; 3-01-00-02161 Reference); 1,3, propylene sulphate; trimethylene sulphate; Schembl51770; Dtxsid4061460; propano-1,3-DIYL sulfate; propylene sulphate, 1,3-, propano, 1,3, sulphate, propylene, 1,3, Sulphate, 1,3-; 1,3,2Lambda, dioxathiane, 2,2, Dione, mfcd00801144; sulphuric acidum 1,3-propaediyl Ester; 1,3,2Lambda6, dioxathiane, 2,2-Dione, Akos015907881, 1,3, propa, Akos015907881, 1,3, Akos015907881; XCVIII%; BS, (XXX) XXXIII, LS, (CXX) CCXCVIII, CS-(CCIV) DLVI; D4427; Ft-(LXXVII) LX; F20412; En300-1725068; W (CVIII) DCCLIII; Q27290765

1,3,2-dioxathiane 2,2-Dioxide proprietas eget

● species / color: albus crystallum pulveris
● Vapor pressura: 0.0589MMMMHG ad XXV ° C
● Melting Point: 58-62ºC
● refractive index: 1.5500 (estimate)
● ferveret punctum: 240.4ºC ad DCCLX Mmhg
● Flash Point: 99.2ºC
● Psa:60.98000
● Density: 1.452 G / CM3
● Listp: 0,74890

● Xlogp3: -0.2
● hydrogenii vinculum donator comitem: 0
● Hydrogenii Bond acceptor comitem: IV
● Rotatable vinculum comitem: 0
● Missa: 137.99867984
● Gravis Atom comitem: VIII
● Complexity: CXLI

Notitia safty

● Picogram (s):Xn
● Codes DISFECTUS:
● statements: XL
● Salutis statements: 22-36

Utilis

Euge classes:Alii Classes -> SULPHUR Revolutionibus
Canonica ridet:C1cos (o) (o) OC1
Usus:1,3,2, dioxathiane 2,2-dioxide est reagent in synthesis deoxy salaminols per coitu reactionem.

Detailed introductio

1,3,2, dioxathiane 2,2-dioxideest heterocyclic compositum cum eget formula c3h6o2s2. Est etiam notum ut Dithiane Dioxide vel Dioxidane. Et compositis ex sex membered anulum cum tres carbonis atomos, unus oxygeni atom et duos sulphure atomos.
Dithiane dioxide habet an interesting structuram et reactivity ex praesentia sulphuris et oxygeni atomi in circulum. Est late usus est in versatile aedificium obstructionum et medium in organicum synthesim. Et compositis est praesertim uti ad suum facultatem subeundum variis eget profectae, faciens illud a valuable resource in progressionem organicum componit.
Unum maxime applicationem ex 1,3,2-dioxathiane 2,2, dioxide est usus in synthesim de sulphuris, quibus organicum moleculis. Potest agere idoneam precursor praeparatio variis heterocyclic componit. In compositis partilibus in nucleophilic addita, anulus-foramen motus, et oxidations, faciens illud a versatile tool in organicum elit.
Praeterea, Dithiane dioxide ludit a significant partes in agro medicinales elit. Quidam derivationes huius compositis demonstratum antimicrobial et antifungal actiones igitur sunt de interest in developing potentiale medicinales agentibus.
Et unique structuram et reactivity exemplaria ex 1,3,2, dioxathiane 2,2-dioxide facere quod essentiale compositis in organicum synthesim et medicinales investigationis. Eius versatility in variis eget reactiones et potentiale biologicum actionibus facere pulchra scopum ad ulteriorem exploratio et application.

Applicatio

1,3,2, dioxathiane 2,2-dioxide habet plures applications in diversis agris. Quidam ex eius notabiles applications includit:
Organicum synthesis:Dithiane dioxide est communiter ut a versatile aedificium obstructionum et medium in organicum synthesis. Potest subire variis eget profectae, ut nuclephilic addita, anulum-foramen motus, et oxidations. Haec reactiones enable synthesis de amplis universa organicum moleculis.
Medicamento Inventionis:Dithiane dioxide et ejus derivationes sunt de interest in agro medicamento inventionis ex potential biologicum actiones. Quidam derivationes ostensum est antimicrobial et antifungal proprietatibus, faciens ea candidati ad progressionem novis therapeutics.
Metallum Coordination Chymicis:Dithiane dioxide potest agere ut chalating ligand, formatam stabile coordinationem complexa variis transitus metallum ions. Haec complexa invenire applications in Catalysis, inorganicis elit et materiae scientia.
Molecular sensoriis:Dithiane dioxide derivationes sunt explored pro eorum sensu elit. Per incorporandi specifica coetus, possunt deprehendere target analyter per mutationes in optical, electrochemical, aut fluorescent properties. Hoc facit eos utile in progressionem de M. sensoriis pro variis applications, comprehendo environmental magna et biomedical Diagnostics.
Polymer Chemistry:Dithiane dioxide potest adhiberi ut monomer ad synthesis Polymer materiae. Et incorporationem in Polymer vincula potest providere unique proprietatibus, ut auctus flexibilitate vel melius eget stabilitatem.
Altiore, ad applications de 1,3,2-dioxathiane 2,2-dioxide span per diversas agros, comprehendo organicum synthesim, medicamento inventa, metallum coordinationem chemistry, et in variis structuram et in variis compositis inquisitores et inquisitores in variis disciplinis.