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169248-97-9

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169248-97-9 Structure

169248-97-9 Structure
IdentificationBack Directory
[Name]

BOC-(TRANS)-4-(3-TRIFLUOROMETHYL-PHENYL)-PYRROLIDINE-3-CARBOXYLIC ACID
[CAS]

169248-97-9
[Synonyms]

BOC-TRANS-DL-PRO(3-TRIFLUOROMETHYLPHENYL)-OH
Boc-trans-DL-b-Pro-4-(3-trifluoromethylphenyl)-OH
BOC-(TRANS)-4-(3-TRIFLUOROMETHYL-PHENYL)-PYRROLID
Boc-trans-DL-beta-Pro-4-(3-trifluoromethylphenyl)-OH
Boc-trans-4-(3-trifluorophenyl)-pyrrolidine-3-carBoxylicacid
BOC-DL-TRANS-4-(3-TRIFLUOROMETHYLPHENYL)PYRROLIDINE-3-CARBOXYLIC ACID
BOC-(TRANS)-4-(3-TRIFLUOROMETHYL-PHENYL)-PYRROLIDINE-3-CARBOXYLIC ACID
Trans-1-Boc-4-(3-(trifluoroMethyl)phenyl)pyrrolidine-3-carboxylic acid
BOC-(±)-TRANS-4-(3-TRIFLUOROMETHYL-PHENYL)-PYRROLIDINE-3-CARBOXYLIC ACID
BOC-(+/-)-TRANS-4-(3-TRIFLUOROMETHYLPHENYL)PYRROLIDINE-3-CARBOXYLIC ACID
4-(3-TrifluoroMethyl-phenyl)-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester
trans-4-[3-(Trifluoromethyl)phenyl]-1,3-pyrrolidinedicarboxylic acid 1-tert-butyl ester
(±)-trans-1-(t-Butoxycarbonyl)-4-(3-trifluoromethylphenyl)pyrrolidine-3-carboxylic acid
trans-1-(tert-Butoxycarbonyl)-4-(3-(trifluoroMethyl)phenyl)pyrrolidine-3-carboxylic acid
(+/-)-TRANS-1-(T-BUTOXYCARBONYL)-4-(3-TRIFLUOROMETHYLPHENYL)PYRROLIDINE-3-CARBOXYLIC ACID
(Tert-Butoxy)Carbonyl (±)-trans-4-(3-trifluoromethyl-phenyl)-pyrrolidine-3-carboxylic acid
(3R,4S)-1-(tert-Butoxycarbonyl)-4-(3-(trifluoroMethyl)phenyl)pyrrolidine-3-carboxylic acid
1-[(2-methylpropan-2-yl)oxy-oxomethyl]-4-[3-(trifluoromethyl)phenyl]-3-pyrrolidinecarboxylic acid
1,3-Pyrrolidinedicarboxylic acid, 4-[3-(trifluoromethyl)phenyl]-, 1-(1,1-dimethylethyl) ester, trans- (9CI)
[Molecular Formula]

C17H20F3NO4
[MDL Number]

MFCD06659291
[MOL File]

169248-97-9.mol
[Molecular Weight]

359.34
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
Hazard InformationBack Directory
[Uses]

Boc-(±)-trans-4-(3-trifluoromethyl-phenyl)-pyrrolidine-3-carboxylic Acid is used to synthesize ring-constrained boropeptide thrombin inhibitors. It is also used to prepare substituted 2H-isoquinolin-1-ones as potent Rho-kinase inhibitors.
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