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CasNo: 36127-17-0
MF: C10H10N2O4S
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2-carbomethoxy-3-tropinone is an intermediate in the synthesis of cocaine isomers at the cocaine receptor.
3-oxo-tropane-2,4-dicarboxylic acid dimethyl ester
(+/-)-2-(carbomethoxy)-3-tropinone
tropinone
Conditions | Yield |
---|---|
With phosphate buffer; In water; at 20 ℃; for 24h; pH=8.0;
|
55% 13% |
tropinone
carbonic acid dimethyl ester
(+/-)-2-(carbomethoxy)-3-tropinone
Conditions | Yield |
---|---|
With methanol; sodium hydride; In cyclohexane; for 1.75h; Heating;
|
80% |
The CAS number of 2-CARBOMETHOXY-3-TROPINONE is 36127-17-0.
More information of 2-CARBOMETHOXY-3-TROPINONE 36127-17-0 are:
CAS Number |
36127-17-0 |
Density |
1.173 g/cm3 |
Melting Point |
104℃ (approx) |
Boiling Point |
294.108 °C at 760 mmHg |
Flash Point |
131.672 °C |
Vapor Pressure |
0.00166mmHg at 25°C |
Refractive Index |
1.502 |
PSA |
46.61000 |
LogP |
0.14910 |
Pka |
10.89±0.20(Predicted) |
Description |
2-Carbomethoxy-3-tropinone is a chemical compound characterized by a tropane ring structure with a carbomethoxy group and a ketone functional group, commonly used as an intermediate in the synthesis of various pharmaceuticals. |
Use |
2-Carbomethoxy-3-tropinone is a key intermediate in the synthesis of cocaine and its analogues. |
Synonyms for 2-CARBOMETHOXY-3-TROPINONE 36127-17-0:1αH,5αH-Tropane-2-carboxylic acid, 3-oxo-, methyl ester (8CI);2-Tropanecarboxylic acid, 3-oxo-, methyl ester (6CI);2-(Methoxycarbonyl)-3-tropanone;8-Methyl-3-oxo-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester;NSC72911;
The chemical formula of 2-CARBOMETHOXY-3-TROPINONE is C10H10N2O4S which containing 10 Carbon atoms,10 Hydrogen atoms,2 Nitrogen atoms,4 Oxygen atoms and 1 Sulfur atoms,and the molecular weight of 2-CARBOMETHOXY-3-TROPINONE is 197.234.
2-Carbomethoxytropinone (2-CMT) is a commonly used organic intermediate in the synthesis of cocaine and its analogues.
InChI:InChI=1/C10H15NO3/c1-11-6-3-4-7(11)9(8(12)5-6)10(13)14-2/h6-7,9H,3-5H2,1-2H3
Relevant articles related to 2-CARBOMETHOXY-3-TROPINONE:
Article |
Source |
New classes of potent and bioavailable human renin inhibitors |
Remen, L'ubos,Bezencon, Olivier,Richard-Bildstein, Sylvia,Bur, Daniel,Prade, Lars,Corminboeuf, Olivier,Boss, Christoph,Grisostomi, Corinna,Sifferlen, Thierry,Strickner, Panja,Hess, Patrick,Delahaye, Stephane,Treiber, Alexander,Weller, Thomas,Binkert, Christoph,Steiner, Beat,Fischli, Walter body text, p. 6762 - 6765 (2010/06/12) |
Novel asymmetric dealkoxycarbonylation of 3-oxo-8-azabicyclo[3.2.1]- octane-2,4-dicarboxylates using porcine liver esterase: A new route to (-)- anhydroecgonine methyl ester |
Node, Manabu,Nakamura, Soichi,Nakamura, Daisaku,Katoh, Takahiro,Nishide, Kiyoharu , p. 5357 - 5360 (2007/10/03) |
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