Basic Information | Post buying leads | Suppliers |
Name |
PROXIL |
EINECS | N/A |
CAS No. | 59209-40-4 | Density | 1.22g/cm3 |
PSA | N/A | LogP | N/A |
Solubility | N/A | Melting Point |
N/A |
Formula | C46H58ClN5O8•2C4H4O4 | Boiling Point | 900.4°Cat760mmHg |
Molecular Weight | 1076.70 | Flash Point | 498.3°C |
Transport Information | N/A | Appearance | N/A |
Safety | Poison by ingestion, intraperitoneal, and subcutaneous routes. An experimental teratogen. Other experimental reproductive effects. When heated to decomposition it emits toxic fumes of Cl− and NOx. An anti-inflammatory agent. | Risk Codes | N/A |
Molecular Structure | Hazard Symbols | N/A | |
Synonyms |
N/A |
IUPAC Name: (Z)-But-2-enedioic acid; 3-[4-[2-[2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetyl]oxyethyl]piperazin-1-yl]propyl 4-benzamido-5-(dipropylamino)-5-oxopentanoate
The molecular formula of Proxil (CAS NO.59209-40-4) is C46H58ClN5O8.2C4H4O4.
The molecular weight of Proxil (CAS NO.59209-40-4) is 1076.578740.
Synonyms of Proxil (CAS NO.59209-40-4): (±)-2-[4-[3-[[4-Benzamido-5-(dipropylamino)glutaryl]oxy]propyl]-1-piperazinyl]ethyl 1-(p-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetate, compound with maleic acid (1:2) ; 1H-Indole-3-acetic acid, 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-, 2-[4-[3-[[4-(benzoylamino)-5-(dipropylamino)-1,5-dioxopentyl]oxy]propyl]-1-piperazinyl]ethyl ester, (+-)-, (Z)-2-butenedioate (1:2)
Enthalpy of Vaporization: 130.93 kJ/mol
Index of Refraction: 1.592
EINECS: 261-656-3
Density: 1.22 g/ml
Flash Point: 498.3 °C
Boiling Point: 900.4 °C
Proxil (CAS NO.59209-40-4) is used as chemical reagent, organic intermediates, fine chemicals, pharmaceutical research and development.
1. | orl-rat LD50:170 mg/kg | OYYAA2 Oyo Yakuri. Pharmacometrics. 32 (1986),1173. | ||
2. | ipr-rat LD50:247 mg/kg | OYYAA2 Oyo Yakuri. Pharmacometrics. 32 (1986),1173. | ||
3. | scu-rat LD50:332 mg/kg | OYYAA2 Oyo Yakuri. Pharmacometrics. 32 (1986),1173. | ||
4. | orl-mus LD50:67 mg/kg | OYYAA2 Oyo Yakuri. Pharmacometrics. 32 (1986),1173. | ||
5. | ipr-mus LD50:243 mg/kg | OYYAA2 Oyo Yakuri. Pharmacometrics. 32 (1986),1173. |
Poison by ingestion, intraperitoneal, and subcutaneous routes. An experimental teratogen. Other experimental reproductive effects. When heated to decomposition it emits toxic fumes of Cl− and NOx. An anti-inflammatory agent.