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5-Methyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-2H-benzo[1,4]oxazine is a complex organic compound with the molecular formula C14H21BO4N. It is a derivative of benzo[1,4]oxazine, a heterocyclic compound with a benzene ring fused to an oxazine ring. The molecule features a methyl group at the 5-position, a 3,4-dihydro structure, and a 4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl group at the 6-position. This latter group is a boron-containing moiety that is often used in Suzuki-Miyaura cross-coupling reactions, a type of carbon-carbon bond-forming reaction in organic synthesis. The compound's structure and functional groups make it a potentially useful intermediate in the synthesis of more complex molecules, particularly in the pharmaceutical and agrochemical industries.

1154740-49-4

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1154740-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1154740-49-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,4,7,4 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1154740-49:
(9*1)+(8*1)+(7*5)+(6*4)+(5*7)+(4*4)+(3*0)+(2*4)+(1*9)=144
144 % 10 = 4
So 1154740-49-4 is a valid CAS Registry Number.

1154740-49-4Downstream Products

1154740-49-4Relevant academic research and scientific papers

AZAINDOLE COMPOUNDS AND METHODS FOR TREATING HIV

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, (2013/03/26)

Provided are compounds and pharmaceutically acceptable salts thereof, their pharmaceutical compositions, their methods of preparation, and their use for treating viral infections mediated by a member of the retrovirus family of viruses such as the Human Immunodeficiency Virus (HIV).

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

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, (2009/06/27)

Compounds of formula I : wherein c, R2, R3, R4, R5, R6, R7 and R8 are defined herein, are useful as inhibitors of HIV replication.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

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Page/Page column 54; 56, (2009/06/27)

Compounds of formula (I): wherein R4, R6 and R7 are defined herein, are useful as inhibitors of HIV replication.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

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Page/Page column 64; 66, (2009/06/27)

Compounds of formula (I): wherein c, X, Y, R2, R4 and R5 are defined herein, are useful as inhibitors of HIV replication.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

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Page/Page column 61-62, (2009/06/27)

The present invention relates to compounds of formula (I) wherein c, X, Y, R2, R3, R4 and R6 are as defined herein, compositions and uses thereof for treating human immunodeficiency virus (HIV) infection. In particular, the present invention provides novel inhibitors of HIV integrase, pharmaceutical compositions containing such compounds and methods for using these compounds in the treatment of HIV infection

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