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CAS No.: | 26400-24-8 |
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Name: | DEHYDROHELIOTRIDINE |
Article Data: | 4 |
Molecular Structure: | |
Formula: | C8H11 N O2 |
Molecular Weight: | 153.181 |
Synonyms: | 1H-Pyrrolizine-7-methanol,2,3-dihydro-1-hydroxy-, (S)- (9CI); Heliotridine, 3,8-didehydro- (8CI); (+)-Dehydroheliotridine;3,8-Dehydroheliotridine; NSC 116336 |
Density: | 1.39g/cm3 |
Boiling Point: | 361.2°Cat760mmHg |
Flash Point: | 172.3°C |
Safety: | Poison by intraperitoneal route. An experimental teratogen. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx. |
PSA: | 45.39000 |
LogP: | 0.41750 |
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IUPAC Name: (1S)-7-(Hydroxymethyl)-2,3-dihydro-1H-pyrrolizin-1-ol
Molecular Formula: C8H11NO2
Molecular Weight: 153.20
Freely Rotating Bonds: 3
Polar Surface Area: 23.39 Å2
Index of Refraction: 1.65
Molar Refractivity: 39.97 cm3
Molar Volume: 109.5 cm3
Polarizability: 15.84 ×10-24 cm3
Surface Tension: 55.5 dyne/cm
Density: 1.39 g/cm3
Flash Point: 172.3 °C
Enthalpy of Vaporization: 64.05 kJ/mol
Boiling Point: 361.2 °C at 760 mmHg
Vapour Pressure: 7.54E-06 mmHg at 25°C
The Cas Register Number of Dehydroheliotridine is 26400-24-8. The chemical synonyms of Dehydroheliotridine (CAS NO.26400-24-8) are (1S)-7-(Hydroxymethyl)-2,3-dihydro-1H-pyrrolizin-1-ol ; 1H-Pyrrolizine-7-methanol, 2,3-dihydro-1-hydroxy-, (1S)- ; Heliotridine, 3,8a-didehydro- .The molecular structure of Dehydroheliotridine (CAS NO.26400-24-8) is.
Dehydroheliotridine (CAS NO.26400-24-8) is used in organic synthesis .
1. | dni-mus:kdy 5 mg/L | CBINA8 Chemico-Biological Interactions. (Elsevier Publishing, P.O. Box 211, Amsterdam C, Netherlands) No. 4,421,71 ,1972. | ||
2. | dnd-dom:kdy 10 mg/L | CBINA8 Chemico-Biological Interactions. 10 (1975),133. | ||
3. | dns-dom:kdy 10 µmol/L | CBINA8 Chemico-Biological Interactions. 13 (1976),243. | ||
4. | dni-dom:kdy 40 mg/L | CBINA8 Chemico-Biological Interactions. 10 (1975),133. | ||
5. | oms-dom:kdy 10 mg/L | CBINA8 Chemico-Biological Interactions. 10 (1975),133. | ||
6. | ipr-rat LDLo:92 mg/kg | CBINA8 Chemico-Biological Interactions. 12 (1976),299. |
Poison by intraperitoneal route. An experimental teratogen. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.