1H-Pyrazole-4-carboxamide, 5-amino-3-[4-[[(5-fluoro-2-methoxybenzoyl)amino]methyl]phenyl]-1-[(1R)-2,2,2-trifluoro-1-methylethyl]-

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1H-Pyrazole-4-carboxamide, 5-amino-3-[4-[[(5-fluoro-2-methoxybenzoyl)amino]methyl]phenyl]-1-[(1R)-2,2,2-trifluoro-1-methylethyl]- Suppliers list
Company Name: ShangHai Caerulum Pharma Discovery Co., Ltd.  
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1H-Pyrazole-4-carboxamide, 5-amino-3-[4-[[(5-fluoro-2-methoxybenzoyl)amino]methyl]phenyl]-1-[(1R)-2,2,2-trifluoro-1-methylethyl]- Basic information
Product Name:1H-Pyrazole-4-carboxamide, 5-amino-3-[4-[[(5-fluoro-2-methoxybenzoyl)amino]methyl]phenyl]-1-[(1R)-2,2,2-trifluoro-1-methylethyl]-
Synonyms:1H-Pyrazole-4-carboxamide, 5-amino-3-[4-[[(5-fluoro-2-methoxybenzoyl)amino]methyl]phenyl]-1-[(1R)-2,2,2-trifluoro-1-methylethyl]-;(R)-Pirtobrutinib;(R)-5-Amino-3-(4-((5-fluoro-2-methoxybenzamido)methyl)phenyl)-1-(1,1,1-trifluoropropan-2-yl)-1H-pyrazole-4-carboxamide;Florfenicol Impurity 18
CAS:2101700-14-3
MF:C22H21F4N5O3
MW:479.43
EINECS:
Product Categories:
Mol File:2101700-14-3.mol
1H-Pyrazole-4-carboxamide, 5-amino-3-[4-[[(5-fluoro-2-methoxybenzoyl)amino]methyl]phenyl]-1-[(1R)-2,2,2-trifluoro-1-methylethyl]- Structure
1H-Pyrazole-4-carboxamide, 5-amino-3-[4-[[(5-fluoro-2-methoxybenzoyl)amino]methyl]phenyl]-1-[(1R)-2,2,2-trifluoro-1-methylethyl]- Chemical Properties
Boiling point 619.2±55.0 °C(Predicted)
density 1.44±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : 200 mg/mL (417.16 mM; Need ultrasonic)
pka13.32±0.46(Predicted)
form Solid
color Light yellow to yellow
Safety Information
MSDS Information
1H-Pyrazole-4-carboxamide, 5-amino-3-[4-[[(5-fluoro-2-methoxybenzoyl)amino]methyl]phenyl]-1-[(1R)-2,2,2-trifluoro-1-methylethyl]- Usage And Synthesis
Uses(R)-Pirtobrutinib ((R)-LOXO-305) is a less active enantiomer of Pirtobrutinib. Pirtobrutinib (LOXO-305), a highly selective and non-covalent next generation BTK inhibitor, inhibits diverse BTK C481 substitution mutations[1].
Biological Activity(R)-Pirtobrutinib ((R)-LOXO-305) is a less active enantiomer of Pirtobrutinib. Pirtobrutinib (LOXO-305), a highly selective and non-covalent next generation BTK inhibitor, inhibits diverse BTK C481 substitution mutations[1].
References[1]. Gomez E B , et al. Loxo-305, a Highly Selective and Non-Covalent Next Generation BTK Inhibitor, Inhibits Diverse BTK C481 Substitution Mutations[J]. Blood, 2019, 134(Supplement_1):4644-4644.
1H-Pyrazole-4-carboxamide, 5-amino-3-[4-[[(5-fluoro-2-methoxybenzoyl)amino]methyl]phenyl]-1-[(1R)-2,2,2-trifluoro-1-methylethyl]- Preparation Products And Raw materials
Tag:1H-Pyrazole-4-carboxamide, 5-amino-3-[4-[[(5-fluoro-2-methoxybenzoyl)amino]methyl]phenyl]-1-[(1R)-2,2,2-trifluoro-1-methylethyl]-(2101700-14-3) Related Product Information
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