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Substance Name: Beclamide [INN:BAN:DCF]
RN: 501-68-8
UNII: F5N0ALI65V
InChIKey: JPYQFYIEOUVJDU-UHFFFAOYSA-N

Classification Code

  • Drug / Therapeutic Agent

Molecular Formula

  • C10-H12-Cl-N-O

Molecular Weight

  • 197.6638
 
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Names and Synonyms

Name of Substance

  • Beclamide
  • Beclamide [INN:BAN:DCF]

Synonyms

  • 3-Chloro-N-(phenylmethyl)propanamide
  • 4-12-00-02234 (Beilstein Handbook Reference)
  • Beclamid
  • Beclamida
  • Beclamida [INN-Spanish]
  • Beclamide
  • Beclamidum
  • Beclamidum [INN-Latin]
  • Beklamid
  • Benxchlorpropamide
  • Benzchlorpropamid
  • Benzchlorpropamide
  • Benzochlorpropamid
  • Benzylamide
  • BRN 2720702
  • Chloracon
  • Chlorakon
  • Chlorakon (VAN)
  • Chloroethylphenamide
  • Chloropropionamide
  • EINECS 207-927-1
  • Hibicon
  • Khlorakon
  • N-(3-Chloropropionyl)benzylamine
  • N-Benzyl-3-chloropropionamide
  • N-Benzyl-beta-chloropropanamide
  • N-Benzyl-beta-chloropropionamide
  • Neuracen
  • Nidrane
  • NSC 67062
  • Nydran
  • Nydrane
  • Posedrin
  • Posedrine
  • Seclar
  • UNII-F5N0ALI65V

Systematic Names

  • Beclamide
  • N-Benzyl-3-chloropropionamide
  • Propanamide, 3-chloro-N-(phenylmethyl)- (9CI)
  • Propionamide, N-benzyl-3-chloro-

Registry Numbers

CAS Registry Number

  • 501-68-8

FDA UNII

  • F5N0ALI65V

System Generated Number

  • 0000501688

Structure Descriptors

InChI

1S/C10H12ClNO/c11-7-6-10(13)12-8-9-4-2-1-3-5-9/h1-5H,6-8H2,(H,12,13)

InChIKey

JPYQFYIEOUVJDU-UHFFFAOYSA-N

Smiles

c1ccc(cc1)CNC(=O)CCCl

Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mammal (species unspecified) LD50 unreported 1368mg/kg (1368mg/kg)   Pharmaceutical Chemistry Journal Vol. 28, Pg. 452, 1994.
mouse LD50 intraperitoneal 650mg/kg (650mg/kg)   "Psychotropic Drugs and Related Compounds," 2nd ed., Usdin, E., and D.H. Efron, Washington, DC, 1972Vol. -, Pg. 384, 1972.
mouse LD50 oral 1gm/kg (1000mg/kg) BEHAVIORAL: ANTICONVULSANT Pharmaceutical Chemistry Journal Vol. 14, Pg. 99, 1980.
rat LD50 intraperitoneal 770mg/kg (770mg/kg)   Journal of Pharmacology and Experimental Therapeutics. Vol. 107, Pg. 403, 1953.
rat LD50 intravenous 770mg/kg (770mg/kg)   "Psychotropic Drugs and Related Compounds," 2nd ed., Usdin, E., and D.H. Efron, Washington, DC, 1972Vol. -, Pg. 384, 1972.
rat LD50 oral 3200mg/kg (3200mg/kg)   Journal of Pharmacology and Experimental Therapeutics. Vol. 107, Pg. 403, 1953.

Physical Properties

Physical Property Value Units Temp (deg C) Source
Melting Point 94 deg C   EXP
log P (octanol-water) 1.760 (none)   EST
Water Solubility 100 mg/L   EXP
Atmospheric OH Rate Constant 1.58E-11 cm3/molecule-sec 25 EST

Physical property data is provided to ChemIDplus by SRC, Inc.