ChemicalBook--->CAS DataBase List--->627530-84-1

627530-84-1

627530-84-1 Structure

627530-84-1 Structure
IdentificationBack Directory
[Name]

BMS 564929
[CAS]

627530-84-1
[Synonyms]

929
BMS-564
BMS 564929
BMS 564929;BMS564929
BMS-564929;BMS-564;929; BMS 564929
2-chloro-4-((7R,7aS)-7-hydroxy-1,3-dioxotetrahydro-1H-pyrrolo[1,2-c]imidazol-2(3H)-yl)-3-methylbenzonitrile
2-Chloro-3-methyl-4-[(7R,7aS)-tetrahydro-7-hydroxy-1,3-dioxo-1H-pyrrolo[1,2-c]imidazol-2(3H)-yl]benzonitrile
Benzonitrile, 2-chloro-3-methyl-4-[(7R,7aS)-tetrahydro-7-hydroxy-1,3-dioxo-1H-pyrrolo[1,2-c]imidazol-2(3H)-yl]-
[Molecular Formula]

C14H12ClN3O3
[MDL Number]

MFCD15146692
[MOL File]

627530-84-1.mol
[Molecular Weight]

305.72
Chemical PropertiesBack Directory
[Boiling point ]

523.3±60.0 °C(Predicted)
[density ]

1.58±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 50 mg/mL (163.55 mM); Water: < 0.1 mg/mL (insoluble)
[form ]

neat
[pka]

13.38±0.20(Predicted)
[color ]

White to off-white
[BRN ]

11053870
[Major Application]

forensics and toxicology
pharmaceutical (small molecule)
[InChI]

1S/C14H12ClN3O3/c1-7-9(3-2-8(6-16)11(7)15)18-13(20)12-10(19)4-5-17(12)14(18)21/h2-3,10,12,19H,4-5H2,1H3/t10-,12+/m1/s1
[InChIKey]

KEJORAMIZFOODM-PWSUYJOCSA-N
[SMILES]

O=C([C@@]1([H])N2CC[C@H]1O)N(C3=C(C)C(Cl)=C(C#N)C=C3)C2=O
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Hazard InformationBack Directory
[Uses]

BMS-564929 is a selective androgen receptor modulator that induces anabolic effects. Potential use in osteoporosis treatments; SARMs
[in vivo]

In sexually mature, castrated male rats, a well-characterized animal model, BMS-564929 (p.o.) shows substantially more potent activity in the levator ani, exhibiting an ED50 of 0.0009 mg/kg in the levator ani and an ED50 of 0.14 mg/kg in the prostate; a net 160-fold selectivity for muscle vs. prostate. Approximately 100% muscle stimulation is achieved at 0.1 mg/kg, reaching greater than 125% stimulation at 0.3 and 1 mg/kg. Compared with T propionate (TP) in the same model, BMS-564929 is more than 200 times more potent in stimulation of muscle and 80 times more selective for muscle vs. prostate[1].

[storage]

Store at -20°C
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