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`Substance Name: Beclamide [INN:BAN:DCF]
`RN: 501-68-8
`InCthey: JPYQFYIEOUVJDU-UHFFFAOYSA-N
`Classificalion Code
`Elnrug [Therapeutic Agent
`
`Molecular Formula
`@C1fl—H12-Cl—N—O
`Molecular Weight
`19713633
`
`
`
`U
`
`JV
`
`cu
`
`u
`
`I
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`
`\ /
`\ r
`\ r
`\ /
`\ /
`Unlesb Resources
`NarnesA monyrrei
`Regisl'y Nurrbers
`Stumre Desuiphrs
`Toxicity
`Pllyai-l Properies
`
`\
`
`Links to Resoumes
`NLIiI Resources (File Locatnrs)
`EJRTECS
`EJDART
`@TOXLINE
`@EINECS
`@Pubcnem
`E] MeSH
`other Resources (Internet Locators)
`@NIST WebBOOk
`@EF‘A ACTOR
`
`Search for this InCthey on the Web
`
`IDrugF‘ortal
`ElPubMed
`@PubMed Toxicology
`
`@PubMed Cancer
`
`
`
`ElBeclamide [INN:BAN:DCF]
`
`@Benxchlorpropamide
`@Benzchlorpmpamid
`@Benzcniorpmpamide
`ElBenzocnlorpropamid
`@Benzylamide
`[BERN 272nm
`@cnioraoon
`@Chlorakon
`@cnioiakon (VAN)
`
`@Neuiaoen
`@Chloroelnylphenamide
`@Nidrane
`Elchloropropionamide
`@Nsc 67062
`EJEINECS 207—9274
`ENydran
`IHibioon
`
`EiNydrane
`Khloralmn
`EJPosedrin
`IN-{Cl-
`@Poseanne
`Chloropropionylwenzylamine
`ElNeBenzyKiashlompmpionamide @Seclar
`@N-BenZyl-bela-
`@UNILF5NOALI65V
`chloropropanamide
`ElNiBenzyLbelai
`chloropropionarnide
`
`ElNiBenzylaachlorupropionamide
`
`ElPrupanamide, 3£nloroiNi
`(phenylmethyl)- (QCI)
`
`@Propionamide, Nibenzylzli
`chloro—
`
`Names and Synonyms
`Name of Substance
`@Bechmide
`Synonyms
`EGACIIIOIOst
`{phenylmethyhpmpanamide
`534-1243042234 (Beilslein
`Handbook Reference)
`@Bechmid
`_
`E 595m!“
`Efiecmm ['N’mpanshl
`@Beclamide
`@Bec'am'dum
`E] Beclamidum [INNiLatin]
`E] Beklamid
`
`Systematic Names
`E1 Beclamide
`
`Reqislry Numbers
`CA5 Registry Number
`51501-634]
`System Generated Number
`@00U050163i‘]
`
`Structure Descriptors
`Inchl
`1SJC10H12CINOIC11-7—fi-ID(13)12-8-9—4—2—1-343—Eli'h1-5H,6-&H2,(H,12,13)
`Download
`
`Incthey
`JPYQFYIEOUVJDUUHFFFAOYSAN
`Search Ihe wen ldr this IncnIKey
`Smiles
`c1ccc 0C1 CNC(:0)CCCI
`Download
`
`LDED unreported
`
`13fiBmgi'kg
`(1368mgi‘kg)
`LDED inlraperituneal 650mglkg
`(GSOmQ'kg)
`
`
`
`Pharmaceutical Chemistry Journal Vol, 23, Pg 452,
`1994.
`"Psychotropic Drugs and Related Compounds," 2nd ed,
`Usdin, E., and DH. Efren, Washington, DC, 197W0l. 7,
`Pg 3&4, 1972,
`
`http://chem.sis.nIm.nih.gov/chemidplus/rn/501-68-8
`
`Actavis v. Research Corp. Techs.
`|PR2014-01126
`
`RCT EX. 2011 page 1
`
` mammal
`
`
`
`(species
`unspecified)
`mouse
`
`
`
`
`
`Actavis v. Research Corp. Techs.
`IPR2014-01126
`RCT EX. 2011 page 1
`
`
`
`
`
`hfisBEEfiied)
`‘ '””"""'"”’
`'"" "
`
`
`mouse
`LD50 intraperitoneal 650mgflrg
`"Psychotropic Drugs and Related Compounds," 2nd ed.,
`
`
`
`(650mglkg)
`Usdin, E., and DH. Efren, Washington, DC, 1972Vol. 7,
`
`
`
`Pg. 384, 1972.
`
`
`mouse
`LD50 oral
`1gmlkg
`BEHAVIORAL:
`Pharmaceutical Chemislry Journal Vol. 14, Pg. 99, 1900.
`
`
`
`(1000mglkg)
`ANTICONVULSANT
`
`
`rat
`LD50 intraperitoneal FTDmQIkg
`Journal of Pharmacology and Experimental
`
`
`(T70mglkg)
`Therapeutics. Vol. 10?, Pg. 403, 1953.
`
`
`
`Link to PubMed
`
`
`rat
`LD50 intravenous
`FTDmQIkg
`"Psychotropic Drugs and Related Compounds," 2nd ed.,
`
`
`
`(T70mglkg)
`Usdin, E., and DH. Efren, Washington, DC, 1972\n’ol. —,
`
`
`
`Pg. 384, 1972.
`
`
`rat
`LD50 oral
`32DDmgIkg
`Journal of Pharmacology and Experimental
`
`
`
`Therapeutics. Vol. 10?, Pg. 403, 1953.
`(3200mglkg)
`
`
`Link to PubMed
`
`
`
`Physical Properlies
`
`
`Physical Property
`Value
`Unils
`Temp [Ibg C} Sauce
`
`
`94
`deg C
`EXP
`Melting Point
`
`
`
`log P (oclanol—waler)
`1.760
`(none)
`EST
`
`
`Water Solubility
`100
`mgIL
`EXP
`
`
`
`Atmospheric OH Rale Conslant 1.58E—11 cm3lmolecule—sec 25
`EST
`Pivysicaipmpmy dams prm'lhd momma hy amuse Research Corporation
`
`
`
`
`See all available property dalafor lhis compound, hum-g Raina-:5
`
`
`
`
`
`
`
`
`
`
`
`
`
`
` 'le Pike Bethesda MD 30354
`
`http://chem.sis.nIm.nih.gov/chemidplus/rn/501-68-8
`
`Actavis v. Research Corp. Techs.
`|PR2014-01126
`
`RCT EX. 2011 page 2
`
`Actavis v. Research Corp. Techs.
`IPR2014-01126
`RCT EX. 2011 page 2
`
`
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