Productus
III-Acylyl-III-chlorodihydrofurran-II (3h) -one; Cas No.: 2986-00-7
Synonyma: 2986-00-7; III-acetyl-III-chloroxolan-II-unum; III-acetyl-III-chlorodihydrofurran-II (3h-chlorodihydrofuran-III-III-chlorodihydrofuran, III-III-chlorodihydrofuran, III-III-chlorodihydrofuran, III-^-II, III-acetyl-III-chlorodihydro-, III-acetyl-III-chloro-tetrahydrofurran-II-unum; einecs 221-050-1; MFCD08448079; II-Acyll-II-chlorobutyrolactone, Alpha-Acyl-Alpha-Chloro, Gamma-butyrolactone; schembl263371, DTL556425, II-Acyl mma-butyrolactone; Akos006288438, III-acetyl-III-chlorotetrahydrofurran-II-unum; III-chlorotho-III-Acc Tyltetrahhydro-II-Furanone; sicut, (XL) CLXXIII, CS-(CCCVIII) CMXXI, ft-(LXVI) CXCIV, en300-140904; a911999; J-(XVII) DCLXX
III-III-III-choraeyl-chlorodihydrofurr-II (3h) -one
● Vapor pressura: 0.000786MMMMHG ad XXV ° C
● Melting Point: 2.2-3.0 ° C
● ferveret Point: 306.1 ° Cat760MMMHG
● Flash Point: 147.8 ° C
● Psa:43.37000
● Density: 1.33g / CM3
● Listp: 0.49990
● repono temp.refrigerator, in inertes atmosphaera
● Solubility.:chlorform (leviter), Methanol (leviter)
● Xlogp3: 0.6
● hydrogenii vinculum donator comitem: 0
● Hydrogenii Bond acceptor comitem: III
● Rotatable vinculum comitem: I
● Missa: 162.0083718
● Gravis Atom comitem: X
● Complexity: CLXXXIX
Notitia safty
● Picogram (s):
● Codes aleam:
Utilis
Canonica ridet:CC (o) C1 (CCOC1 = o) Cl
Detailed introductio
III-acetyl-III-chlorodihydrofurran-II (3h) -oneEst chemical compositis cum mocecular formula c6h7clo3. Hoc pertinet ad genus of organicum componit notum ut furans, quae sunt propria a quinque-membered anulum continet unum oxygeni atom. In hoc compositis, in Furanum anulus est chlorinated ad in III-situ, et non est acetyl group (ch3co) attachiatus ad III-situ de anulum.
III-Acylyl-III-chlorodihydrofurran-II (3h) -one est colore pallide flavo liquidum fortis odore. Est solutum in organicum solvents sicut ethanol, methanolum et dichloromethane.
Hoc compositis est saepe usus est in aedificationem obstructionum aut medium in organicum synthesim et pharmaceutical vestibulum. Non potest esse creare amplis derivationes et substituit Furanum componit, qui invenies applications in variis industrias.
Est momenti ad tractamus III-acetyl-III-chlorodihydrofurran-II (3h) -one cum caute et sequi oportet salutem protocols, ut sit ancipitia, si non tractari proprie.
Applicatio
Unum potentiale applicationem III-acetyl-III-chlorodihydrofurran-II (3h) -onein agro saporem et odor. Furanum derivationes sunt unique et iucundum odores, faciens valuable ingredientia in formula unguenta, stibia, et cibum flavorings.
Et compositis potest etiam esse ut a incipiens materia ad synthesim of pharmaceuticals et biologically active moleculis. Furanum derivationes sunt inventa ut exhibeant variis pharmacological activities, inter antimicrobial, antiviral, antitumor et anti-inflammatory proprietatibus. Ut talis, III-acetyl-III-chlorodihydrofurran-II (3h) -one potest servire quasi key medium in synthesis harum bioactivae componit.
Ceterum Furanum componit fuisse usus est in progressionem agrochemicals et seges tutela agentibus debitum ad eorum facultatem ad inhibere plant pathogens et pestes. Et unique chemical structuram de III-acetyl-III, chlorodihydrofurran-II (3h) -one facit illud potentiale candidatum ad synthesis talis componit.
Est dignum attendens quod specifica applications of III-acetyl-III-chlorodihydrofurran-II (3h) -one potest variari fretus ongoing investigationis et technicae progressiones in variis industrias.
