1,2-Dithiocane-3,8-diol
Names
[ CAS No. ]:
5244-34-8
[ Name ]:
1,2-Dithiocane-3,8-diol
[Synonym ]:
3,6-dithia-1,8-0ctanediol
1,2-Dithiocane-3,8-diol
MFCD00002911
DITHIOOCTANEDIOL
3,6-dithia-1,8-octandiol
2,2'-(Ethane-1,2-diylbis(sulfanediyl))diethanol
Ethylenedithioethanol
2,2',6,6'-TETRAMETHYL-4,4'-BIPYRIDINE
LINDLAR CATALYST POISON
DITHIAOCTANEDIOL
DithioocataneDiol
1,2-Bis(2-hydroxyethylthio)ethane
2,2'-(Ethylenedithio)diethanol
EINECS 226-045-8
DITHIA-TRIETHYLENEGLYCOL
3,6-Dithia-1,8-octan
DTO
Lindlar catalyst
Chemical & Physical Properties
[ Density]:
1.3±0.1 g/cm3
[ Boiling Point ]:
346.0±42.0 °C at 760 mmHg
[ Melting Point ]:
63-64 °C(lit.)
[ Molecular Formula ]:
C6H14O2S2
[ Molecular Weight ]:
180.288
[ Flash Point ]:
168.3±26.6 °C
[ Exact Mass ]:
180.027863
[ PSA ]:
91.06000
[ LogP ]:
0.94
[ Vapour Pressure ]:
0.0±1.7 mmHg at 25°C
[ Index of Refraction ]:
1.617
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ Hazard Codes ]:
C
[ Safety Phrases ]:
S22-S24/25
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
1
[ HS Code ]:
29309070
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2930909090
[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Articles
Proc. Natl. Acad. Sci. U. S. A. 102(32) , 11179-84, (2005)
Copper is an essential micronutrient that plays a central role for a broad range of biological processes. Although there is compelling evidence that the intracellular milieu does not contain any free ...
Allylation of erythromycin derivatives: introduction of allyl substituents into highly hindered alcohols.J. Org. Chem. 68(23) , 8847-52, (2003)
Functionalized erythromycin 9-oxime derivatives are 6-O-allylated under mild conditions using substituted allyl tert-butyl carbonates under palladium(0) catalysis. This allylation works well where tra...
Asymmetric Total Synthesis of (+)-6-epi-Castanospermine by the Stereoselective Formation of a syn, anti Acetylenic 2-Amino-1, 3-diol Stereotriad. Louvel J, et al.European J. Org. Chem. 2010(15) , 2921-26, (2010)