ChemicalBook--->CAS DataBase List--->20461-99-8

20461-99-8

20461-99-8 Structure

20461-99-8 Structure
IdentificationMore
[Name]

ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE
[CAS]

20461-99-8
[Synonyms]

1,3-DITHIOLANE-2-CARBOXYLIC ACID ETHYL ESTER
ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE
ETHYL GLYOXYLATE ETHYLENE THIOACETAL
GLYOXYLIC ACID ETHYL ESTER ETHYLENE MERCAPTAL
2-Carboethoxy-1,3-dithiolane
2-Carboethoxydithiolane
2-Carboethoxy-1,3-dithiolane~1,3-Dithiolane-2-carboxylicacidethylester~2-Ethoxycarbonyl-1,3-dithiolane~Ethylglyoxyla
Ethyl 1,3-dithiolane-2-carboxylate, GC 99%
1,3-DITHIOLANE-2-CARBOXYLIC ACID ETHYL ESTER 95+%
Ethyl 1,3-dithiolane-2-carboxylate, 98+%
[EINECS(EC#)]

243-837-9
[Molecular Formula]

C6H10O2S2
[MDL Number]

MFCD00005411
[Molecular Weight]

178.27
[MOL File]

20461-99-8.mol
Chemical PropertiesBack Directory
[Appearance]

clear light yellow liquid
[Boiling point ]

85 °C/0.1 mmHg (lit.)
[density ]

1.249 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.539(lit.)
[Fp ]

>230 °F
[storage temp. ]

2-8°C
[form ]

Liquid
[color ]

Clear light yellow
[Specific Gravity]

1.249
[BRN ]

118157
[CAS DataBase Reference]

20461-99-8(CAS DataBase Reference)
Safety DataBack Directory
[Safety Statements ]

S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S24/25:Avoid contact with skin and eyes .
[RIDADR ]

3334
[WGK Germany ]

3
[F ]

8-9
[HS Code ]

29349990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Potassium-->1,2-Ethanedithiol-->ETHYL DIBROMOACETATE
[Preparation Products]

1,3-dithiolan-2-ylmethanol
Hazard InformationBack Directory
[Chemical Properties]

clear light yellow liquid
[General Description]

Ethyl 1,3-dithiolane-2-carboxylate is an α-keto acid equivalent. It participates in the conjugate additions to enones. It is a bulky equivalent of acetate undergoing syn-selective aldol reactions. Anion derived from ethyl 1,3-dithiolane-2-carboxylate participates as nucleophile during the total synthesis of the corynanthe alkaloid dihydrocorynantheol and the formal syntheses of the indole alkaloids tacamonine, rhynchophylline and hirsutine. It also participates in the conjugate addition of enolates to phenylglycinol-derived α,β-unsaturated δ-lactams.
[Purification Methods]

Dissolve the ester in CHCl3, wash it with aqueous K2CO3, twice with H2O, dry it over MgSO4, filter, evaporate and distil the residue in vacuo. [Hermann et al Tetrahedron Lett 2599 1973, Corey & Erickson J Org Chem 36 3553 1971]. [Beilstein 19/7 V 225.]
Spectrum DetailBack Directory
[Spectrum Detail]

ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE(20461-99-8)MS
ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE(20461-99-8)1HNMR
ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE(20461-99-8)13CNMR
ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE(20461-99-8)IR1
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Ethyl 1,3-dithiolane-2-carboxylate, 99%(20461-99-8)
[Alfa Aesar]

Ethyl 1,3-dithiolane-2-carboxylate, 98+%(20461-99-8)
[Sigma Aldrich]

20461-99-8(sigmaaldrich)
[TCI AMERICA]

1,3-Dithiolane-2-carboxylic Acid Ethyl Ester,>97.0%(GC)(20461-99-8)
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