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(R)-4-(dibenzylamino)-3-fluoro-2-methylbutan-2-ol is a chiral compound characterized by its molecular formula of C19H23FNO. It features a tertiary alcohol structure with a fluorine atom and a methyl group on the second carbon of the main chain. (R)-4-(dibenzylamino)-3-fluoro-2-methylbutan-2-ol is further distinguished by the presence of a dibenzylamino group on the fourth carbon, which introduces a benzyl group into the molecule. This unique structural composition may endow (R)-4-(dibenzylamino)-3-fluoro-2-methylbutan-2-ol with potential applications across various fields, including pharmaceuticals, organic synthesis, and chemical research. However, further investigation and experimentation are required to comprehensively determine its uses and potential impacts.

1609545-83-6

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1609545-83-6 Usage

Uses

Used in Pharmaceutical Applications:
(R)-4-(dibenzylamino)-3-fluoro-2-methylbutan-2-ol is used as an active pharmaceutical ingredient for its potential therapeutic properties. (R)-4-(dibenzylamino)-3-fluoro-2-methylbutan-2-ol's unique structure may allow it to interact with biological targets in novel ways, offering new avenues for the treatment of various diseases and conditions.
Used in Organic Synthesis:
In the field of organic synthesis, (R)-4-(dibenzylamino)-3-fluoro-2-methylbutan-2-ol serves as a valuable building block or intermediate for the creation of more complex molecules. Its distinct structural features can be leveraged to synthesize a wide range of compounds with diverse applications, from pharmaceuticals to advanced materials.
Used in Chemical Research:
(R)-4-(dibenzylamino)-3-fluoro-2-methylbutan-2-ol is utilized as a research tool in chemical laboratories. Its unique properties and reactivity make it an interesting subject for studying various chemical reactions and mechanisms, potentially leading to new insights and discoveries in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1609545-83-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,5,4 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1609545-83:
(9*1)+(8*6)+(7*0)+(6*9)+(5*5)+(4*4)+(3*5)+(2*8)+(1*3)=186
186 % 10 = 6
So 1609545-83-6 is a valid CAS Registry Number.

1609545-83-6Relevant academic research and scientific papers

Optimization of Nicotinamides as Potent and Selective IRAK4 Inhibitors with Efficacy in a Murine Model of Psoriasis

Nair, Satheesh,Kumar, Sreekantha Ratna,Paidi, Venkatram Reddy,Sistla, Ramesh,Kantheti, Durgarao,Polimera, Subba Rao,Thangavel, Soodamani,Mukherjee, Amrita Jha,Das, Mitalee,Bhide, Rajeev S.,Pitts, William J.,Murugesan, Natesan,Dudhgoankar, Shailesh,Nagar, Jignesh,Subramani, Siva,Mazumder, Debarati,Carman, Julie A.,Holloway, Deborah A.,Li, Xin,Fereshteh, Mark P.,Ruepp, Stefan,Palanisamy, Kamalavenkatesh,Mariappan, T. Thanga,Maddi, Srinivas,Saxena, Ajay,Elzinga, Paul,Chimalakonda, Anjaneya,Ruan, Qian,Ghosh, Kaushik,Bose, Sucharita,Sack, John,Yan, Chunhong,Kiefer, Susan E.,Xie, Dianlin,Newitt, John A.,Saravanakumar, S. Pon,Rampulla, Richard A.,Barrish, Joel C.,Carter, Percy H.,Hynes, John

supporting information, p. 1402 - 1409 (2020/07/02)

IRAK4 is an attractive therapeutic target for the treatment of inflammatory conditions. Structure guided optimization of a nicotinamide series of inhibitors has been expanded to explore the IRAK4 front pocket. This has resulted in the identification of co

HETEROARYL SUBSTITUTED AMINOPYRIDINE COMPOUNDS

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Page/Page column 117; 118, (2017/01/09)

Disclosed are compounds of Formula (I) Formula(I) or salts thereof, wherein HET is a heteroaryl selected from oxazolyl, pyrazolyl, imidazo[l,2-b]pyridazin-3-yl, and pyrazolo[l,5-a]pyrimidin-3-yl, wherein said heteroaryl is attached to the pyridinyl group in the compound of Formula (I) by a carbon ring atom in the heteroaryl and wherein said heteroaryl is substituted with zero to 2 Rb; and R1, R3, and Rb are define herein. Also disclosed are methods of using such compounds as modulators of IRAK4, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing inflammatory and autoimmune diseases, or in the treatment of cancer.

HETEROARYL SUBSTITUTED NICOTINAMIDE COMPOUNDS

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Paragraph 0395, (2015/07/15)

Disclosed are compounds of Formula (I) or salts thereof, wherein: HET is a heteroaryl selected from pyrazolyl, indolyl, pyrrolo[2,3-b]pyridinyl, pyrrolo[2,3-d]pyrimidinyl, pyrazolo[3,4-b]pyridinyl, pyrazolo[3,4-d]pyrimidinyl, 2,3-dihydro-1H-pyrrolo[2,3-b]pyridinyl, imidazo[4,5-b]pyridinyl, and purinyl, wherein said heteroaryl is substituted with Ra and Rb; and R1 and R2 are define herein. Also disclosed are methods of using such compounds as modulators of IRAK4, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing inflammatory and autoimmune diseases.

HETEROARYL SUBSTITUTED PYRIDYL COMPOUNDS USEFUL AS KINASE MODULATORS

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Paragraph 00234, (2019/03/15)

Compounds having the following formula (I) or a stereoisomer or a pharmaceutically-acceptable salt thereof, wherein R2 is a monocyclic heteroaryl group, and R1, R3, R4, R5 and R6 are as defined herein, are useful as kinase modulators, including IRAK-4 inhibition.

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