ethyl 1,3-dithiolane-2-carboxylate

Modify Date: 2025-08-25 18:20:18

ethyl 1,3-dithiolane-2-carboxylate Structure
ethyl 1,3-dithiolane-2-carboxylate structure
Common Name ethyl 1,3-dithiolane-2-carboxylate
CAS Number 20461-99-8 Molecular Weight 178.27200
Density 1.249 g/mL at 25 °C(lit.) Boiling Point 85 °C0.1 mm Hg(lit.)
Molecular Formula C6H10O2S2 Melting Point N/A
MSDS USA Flash Point >230 °F

 Names

Name ethyl 1,3-dithiolane-2-carboxylate
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.249 g/mL at 25 °C(lit.)
Boiling Point 85 °C0.1 mm Hg(lit.)
Molecular Formula C6H10O2S2
Molecular Weight 178.27200
Flash Point >230 °F
Exact Mass 178.01200
PSA 76.90000
LogP 1.35560
Vapour Pressure 0.013mmHg at 25°C
Index of Refraction n20/D 1.539(lit.)
InChIKey OMCSHTHLIQOHDD-UHFFFAOYSA-N
SMILES CCOC(=O)C1SCCS1

 Safety Information

Personal Protective Equipment Eyeshields;Gloves
Safety Phrases S23-S24/25
RIDADR 3334
WGK Germany 3
HS Code 2934999090

 Synthetic Route

~%

ethyl 1,3-dithiolane-2-carboxylate Structure

ethyl 1,3-dithi...

CAS#:20461-99-8

Literature: Journal of the Indian Chemical Society, , vol. 5, p. 457 Chem. Zentralbl., , vol. 99, # II p. 2254

~%

ethyl 1,3-dithiolane-2-carboxylate Structure

ethyl 1,3-dithi...

CAS#:20461-99-8

Literature: Journal of the Indian Chemical Society, , vol. 5, p. 546 Chem. Zentralbl., , vol. 99, # II p. 2253 Journal of the Indian Institute of Science, Section A, vol. 11, p. 228 Chem. Zentralbl., , vol. 100, # I p. 1697

~79%

ethyl 1,3-dithiolane-2-carboxylate Structure

ethyl 1,3-dithi...

CAS#:20461-99-8

Literature: Lissel, Manfred Liebigs Annalen der Chemie, 1982 , # 9 p. 1589 - 1601

~%

ethyl 1,3-dithiolane-2-carboxylate Structure

ethyl 1,3-dithi...

CAS#:20461-99-8

Literature: Journal of the Indian Institute of Science, , vol. 11, p. 227,229 Chem. Zentralbl., , vol. 99, # II p. 2253

 Customs

HS Code 2934999090
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles5

More Articles
General strategy for the syntheses of corynanthe, tacaman, and oxindole alkaloids.

J. Org. Chem. 71(17) , 6547-61, (2006)

We report herein the total synthesis of the corynanthe alkaloid dihydrocorynantheol and the formal syntheses of the indole alkaloids tacamonine, rhynchophylline, and hirsutine. The strategies for asse...

Stereodivergent synthesis of enantiopure cis- and trans-3-Ethyl-4-piperidineacetates.

Org. Lett. 4(16) , 2787-90, (2002)

[reaction: see text] Starting from a common chiral bicyclic lactam 11, enantiopure trans- or cis-3-ethyl-4-piperidineacetate derivatives are obtained by conjugate addition of an enolate or a cuprate t...

H. Paulson, W. Koebernick

Chem. Ber. 110 , 2127, (1977)

 Synonyms

2-Carboethoxydithiolane
1,3-Dithiolane-2-carboxylic Acid Ethyl Ester
Ethyl-1,3-dithiolan-2-carboxylat
Ethyl 1,3-dithiolane-2-carboxylate
ethyl dithiolane-2-carboxylate
2-ethoxycarbonyl-1,3-dithiolane
ethyl 2,2-(1,3-dithiolane-2-yl)acetate
MFCD00005411
EINECS 243-837-9
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