bromadiolone

Chinese: 溴敌隆French: bromadiolone (n.f.)Russian: бромадиолон


Status: ISO 1750 (published)
IUPAC PIN: mixture comprised of 80–100% rac-3-[(1R,3S)-3-(4′-bromo[1,1′-biphenyl]-4-yl)-3-hydroxy-1-phenylpropyl]-4-hydroxy-2H-1-benzopyran-2-one and 20–0% of the rac-(1R,3R)-isomers
IUPAC name: mixture comprised of 80–100% 3-[(1RS,3SR)-3-(4′-bromobiphenyl-4-yl)-3-hydroxy-1-phenylpropyl]-4-hydroxy-2H-chromen-2-one and 20–0% of the (1RS,3RS)-isomers
1979 Rules:
mixture comprised of 80–100% 3-[(1RS,3SR)-3-(4′-bromobiphenyl-4-yl)-3-hydroxy-1-phenylpropyl]-4-hydroxycoumarin and 20–0% of the (1RS,3RS)-isomers
CAS name: 3-[3-(4′-bromo[1,1′-biphenyl]-4-yl)-3-hydroxy-1-phenylpropyl]-4-hydroxy-2H-1-benzopyran-2-one
CAS Reg. No.: 28772-56-7
Formula: C30H23BrO4
Activity: rodenticides (coumarin rodenticides)
Notes: The name “bropropdifacoum” is used in South Africa.
The CAS Registry Number of the major component is 198015-14-4.
The mixture of 80–100% (1RS,3RS)-isomers and 20–0% (1RS,3SR)-isomers has the ISO common name alpha-bromadiolone.
Structure: Structural formula of bromadiolone
Pronunciation: brō-ma--ō-lōn  Guide to British pronunciation
InChIKey: LQAGAOMQXARIFO-YORONTHLSA-N (major component)
InChI: InChI=1S/2C30H23BrO4/c2*31-23-16-14-20(15-17-23)19-10-12-22(13-11-19)26(32)18-25(21-6-2-1-3-7-21)28-29(33)24-8-4-5-9-27(24)35-30(28)34/h2*1-17,25-26,32-33H,18H2/t2*25-,26+/m10/s1 (major component)

A data sheet from the Compendium of Pesticide Common Names