Chemical Properties of Tetrazepam M (norhydroxy-), hydrolysis, acetylated

Tetrazepam M (norhydroxy-), hydrolysis, acetylated

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InChI
InChI=1S/C17H18ClNO4/c1-10(20)19-15-8-7-12(18)9-14(15)17(22)13-5-3-4-6-16(13)23-11(2)21/h5,7-9,16H,3-4,6H2,1-2H3,(H,19,20)
InChI Key
FKYVTMBWEWJAOV-UHFFFAOYSA-N
Formula
C17H18ClNO4
SMILES
CC(=O)Nc1ccc(Cl)cc1C(=O)C1=CCCCC1OC(C)=O
Molecular Weight1
335.78
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Physical Properties

Property Value Unit Source
Δf -184.11 kJ/mol Joback Calculated Property
Δfgas -512.22 kJ/mol Joback Calculated Property
Δfus 41.00 kJ/mol Joback Calculated Property
Δvap 91.89 kJ/mol Joback Calculated Property
log10WS -4.67 Crippen Calculated Property
logPoct/wat 3.523 Crippen Calculated Property
McVol 244.270 ml/mol McGowan Calculated Property
Pc 2113.89 kPa Joback Calculated Property
Inp 2500.00 NIST
Tboil 920.32 K Joback Calculated Property
Tc 1159.22 K Joback Calculated Property
Tfus 608.07 K Joback Calculated Property
Vc 0.918 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [731.32; 781.23] J/mol×K [920.32; 1159.22] Show Hide
Cp,gas 731.32 J/mol×K 920.32 Joback Calculated Property
Cp,gas 742.95 J/mol×K 960.14 Joback Calculated Property
Cp,gas 753.21 J/mol×K 999.95 Joback Calculated Property
Cp,gas 762.13 J/mol×K 1039.77 Joback Calculated Property
Cp,gas 769.75 J/mol×K 1079.59 Joback Calculated Property
Cp,gas 776.11 J/mol×K 1119.40 Joback Calculated Property
Cp,gas 781.23 J/mol×K 1159.22 Joback Calculated Property

Similar Compounds

Tetrazepam M (hydroxy-), isomer 1, hydrolysis, acetylated. Uridine, 2'-O-acetyl, 3',5'-bis-O-TBDMS. Uridine, 2'-O-TBDMS, 3'-O-acetyl, 5'-O-TBDMS. Uridine, 2'-O-TBDMS, 3',5'-bis-O-acetyl. Uridine, 2',3'-bis-O-acetyl, 5'-O-TBDMS. Buprenorphine. Deserpidine. Paclitaxel. Ergotaman-3',6',18-trione, 9,10-dihydro-12'-hydroxy-2'-methyl-5'-(phenylmethyl)-, (5'«alpha»,10«alpha»)-. Ergotamine. Ergocristine. Codeine-propionyl. Ajmaline. Galantamin. 3-propionyl-morphine.

Find more compounds similar to Tetrazepam M (norhydroxy-), hydrolysis, acetylated.

Sources

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