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  • Product Name:   2H-1,4-Benzodiazepin-2-one,5-(2-fluorophenyl)-1,3-dihydro-1-methyl-7-nitro-
  • Synonyms:   2H-1,4-Benzodiazepin-2-one,5-(o-fluorophenyl)-1,3-dihydro-1-methyl-7-nitro- (7CI,8CI);5-(2-Fluorophenyl)-1,3-dihydro-1-methyl-7-nitro-2H-1,4-benzodiazepin-2-one;5-(2-Fluorophenyl)-1-methyl-7-nitro-1,3-dihydrobenzo[e][1,4]diazepin-2-one;5-(o-Fluorophenyl)-1,3-dihydro-1-methyl-7-nitro-2H-1,4-benzodiazepin-2-one;7-Nitro-1-methyl-5-(2-fluorophenyl)-3H-1,4-benzodiazepin-2(1H)-one;Flunidazepam;Flunipam;Flunitrazepam;Fluridrazepam;Narcozep;Ro 5-4200;Rohypnol;Roipnol;Silece;
  • CAS No.:   1622-62-4
  • Molecular Formula:   C16H12FN3O3
  • Molecular Weight :   313.31
  • Specification :   
  • Place of Origin:   China
  • Appearance :   

Description of 2H-1,4-Benzodiazepin-2-one,5-(2-fluorophenyl)-1,3-dihydro-1-methyl-7-nitro-

Detail of > 1622-62-4

  • MSDS Download
  • CAS Number:
  • 1622-62-4
  • Name:
  • 2H-1,4-Benzodiazepin-2-one,5-(2-fluorophenyl)-1,3-dihydro-1-methyl-7-nitro-

  • Superlist Name:
  • Flunitrazepam
  • Formula:
  • C16H12FN3O3
  • Molecular Structure:
  • Synonyms:
  • 2H-1,4-Benzodiazepin-2-one,5-(o-fluorophenyl)-1,3-dihydro-1-methyl-7-nitro- (7CI,8CI);5-(2-Fluorophenyl)-1,3-dihydro-1-methyl-7-nitro-2H-1,4-benzodiazepin-2-one;5-(2-Fluorophenyl)-1-methyl-7-nitro-1,3-dihydrobenzo[e][1,4]diazepin-2-one;5-(o-Fluorophenyl)-1,3-dihydro-1-methyl-7-nitro-2H-1,4-benzodiazepin-2-one;7-Nitro-1-methyl-5-(2-fluorophenyl)-3H-1,4-benzodiazepin-2(1H)-one;Flunidazepam;Flunipam;Flunitrazepam;Fluridrazepam;Narcozep;Ro 5-4200;Rohypnol;Roipnol;Silece;
  • Molecular Weight:
  • 313.31
  • EINECS:
  • 216-597-8
  • Density:
  • 1.39g/cm3
  • Melting Point:
  • 166-167 °C
  • Boiling Point:
  • 540.9°Cat760mmHg
  • Flash Point:
  • 280.9°C
  • Solubility:
  • 45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 1 mg/mL
  • Appearance:
  • UN 1230 3/PG 2
  • Hazard Symbols:
  • HarmfulXnToxicTFlammableF
  • Risk Codes:
  • 22-36-39/23/24/25-23/24/25-11
  • Safety:
  • Moderately toxic by ingestion and intraperitoneal routes. An experimental teratogen. Human reproductive effects by ingestion and intramuscular routes: Apgar score of newborn and other neonatal and postnatal effects. Experimental reproductive effects. Mutation data reported. Human systemic effects by ingestion: coma. Used as a hypnotic agent. Note: This is a controlled substance (depressant) listed in the U.S. Code of Federal Regulations, Title 21 Part 1308.14 (1985). When heated to decomposition it emits toxic fumes of F and NOx.Details

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