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4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indoline is a complex organic compound that serves as a valuable intermediate in the field of organic synthesis. It is characterized by a unique structure, featuring a 1,3,2-dioxaborolane moiety attached to the 4-position of an indoline ring. This chemical is widely used in Suzuki-Miyaura cross-coupling reactions, a powerful method for the formation of carbon-carbon bonds. The presence of the 1,3,2-dioxaborolane group enhances the reactivity of the molecule, making it a preferred choice for the synthesis of various biologically active compounds and pharmaceuticals. Its stability and ease of handling further contribute to its utility in the synthesis of complex organic molecules.

1622173-47-0

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1622173-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1622173-47-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,2,1,7 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1622173-47:
(9*1)+(8*6)+(7*2)+(6*2)+(5*1)+(4*7)+(3*3)+(2*4)+(1*7)=140
140 % 10 = 0
So 1622173-47-0 is a valid CAS Registry Number.

1622173-47-0Relevant academic research and scientific papers

IMMUNOMODULATORS, COMPOSITIONS AND METHODS THEREOF

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Page/Page column 45, (2019/10/30)

Disclosed are compounds of Formula (I), methods of using the compounds as immunomodulators, and pharmaceutical compositions comprising such compounds. The compounds are useful in treating, preventing or ameliorating diseases or disorders such as cancer or

TRICYCLIC HETEROCYCLIC COMPOUNDS AS PHOSPHOINOSITIDE 3-KINASE INHIBITORS

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Page/Page column 48; 49, (2017/03/14)

The invention relates to a compound of formula I: (I) or a pharmaceutically acceptable salt thereof and/or stereoisomers thereof. The compounds of the invention are useful in therapy.

N-SUBSTITUTED HETEROCYCLIC DERIVATIVES AS KINASE INHIBITORS

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Page/Page column 24, (2014/09/03)

The present invention provides N-substituted novel heterocyclic derivatives of formula (I) as protein kinase inhibitors, in which R1, R2 and 'n' have the same meanings given in the specification, and pharmaceutically acceptable salts

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