ethyl 1,3-dithiolane-2-carboxylate structure
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Common Name | ethyl 1,3-dithiolane-2-carboxylate | ||
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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 |
Name | ethyl 1,3-dithiolane-2-carboxylate |
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Synonym | More Synonyms |
Density | 1.249 g/mL at 25 °C(lit.) |
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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.) |
Personal Protective Equipment | Eyeshields;Gloves |
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Safety Phrases | S23-S24/25 |
RIDADR | 3334 |
WGK Germany | 3 |
HS Code | 2934999090 |
~% 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-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-dithi... CAS#:20461-99-8 |
Literature: Lissel, Manfred Liebigs Annalen der Chemie, 1982 , # 9 p. 1589 - 1601 |
~% 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 |
Precursor 4 | |
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DownStream 5 | |
HS Code | 2934999090 |
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Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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... |
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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... |
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H. Paulson, W. Koebernick
Chem. Ber. 110 , 2127, (1977)
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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 |