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51931-66-9

51931-66-9 Structure

51931-66-9 Structure
IdentificationBack Directory
[Name]

ethyl trans-2-(dimethylamino)-1-phenylcyclohex-3-ene-1-carboxylate
[CAS]

51931-66-9
[Synonyms]

Dea no. 9750
Tilidate [ban]
trans-Tilidine
Einecs 257-522-9
ethyl trans-2-(dimethylamino)-1-phenylcyclohex-3-ene-1-carboxylate
Ethyl trans-2-(dimethylamino)-1-phenyl-3-cyclohexene-1-carboxylate
3-Cyclohexene-1-carboxylic acid, 2-(dimethylamino)-1-phenyl-, ethyl ester, trans-
3-Cyclohexene-1-carboxylic acid, 2-(dimethylamino)-1-phenyl-, ethyl ester, (1R,2S)-rel-
[EINECS(EC#)]

257-522-9
[Molecular Formula]

C17H23NO2
[MOL File]

51931-66-9.mol
[Molecular Weight]

273.37
Chemical PropertiesBack Directory
[Boiling point ]

96 °C(Press: 0.01 Torr)
[density ]

1.06±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C
[pka]

8.26±0.40(Predicted)
[InChI]

1S/C17H23NO2/c1-4-20-16(19)17(14-10-6-5-7-11-14)13-9-8-12-15(17)18(2)3/h5-8,10-12,15H,4,9,13H2,1-3H3/t15-,17?/m1/s1
[InChIKey]

WDEFBBTXULIOBB-LDCVWXEPSA-N
[SMILES]

N([C@H]1C(CCC=C1)(c2ccccc2)C(=O)OCC)(C)C
Safety DataBack Directory
[Symbol(GHS) ]

Health Hazard (GHS08)Exclamation Mark (GHS07)
GHS08,GHS07
[Signal word ]

Danger
[Hazard statements ]

H332-H302-H373-H312-H334
[Precautionary statements ]

P260-P314-P501-P280-P302+P352-P312-P322-P363-P501-P261-P285-P304+P341-P342+P311-P501-P264-P270-P301+P312-P330-P501-P261-P271-P304+P340-P312
[WGK Germany ]

WGK 3
[REACH Registrations]

Active
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Resp. Sens. 1
STOT RE 2
Hazard InformationBack Directory
[Uses]

Tilidine is an opioid used primarily as a painkiller it inhibits the enzyme adenylyl cyclase.
[Definition]

ChEBI: Dextilidine is an ethyl 2-(dimethylamino)-1-phenylcyclohex-3-ene-1-carboxylate that has S configuration at the carbon bearing the phenyl group and R configuration at the carbon bearing the dimethylamino group. The opioid analgesic tilidine is the racemate comprising equimolar amounts of dextilidine and its enantiomer, ent-dextilidine. A prodrug, tilidine is converted by the liver to the active analgesic, nortilidine; virtually all of the opioid activity resides in the (1S,2R) isomer (i.e. the isomer derived from dextilidine). It has a role as an opioid analgesic and a prodrug. It is an enantiomer of an ent-dextilidine.
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