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2H-1,4-Benzoxazine, 3,4-dihydro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)is a complex organic compound that is part of the benzoxazine family. It is characterized by its 3,4-dihydro derivative structure and the presence of a boron-containing functional group at the 6th position. This unique structure and the boron-containing group make it a potentially versatile building block for the synthesis of new compounds with specific properties and applications in various fields such as chemistry, material science, and pharmaceuticals.

1155264-46-2

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1155264-46-2 Usage

Uses

Used in Chemical Synthesis:
2H-1,4-Benzoxazine, 3,4-dihydro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)is used as a versatile building block in chemical synthesis for the creation of new compounds with specific properties. The boron-containing group offers opportunities for further functionalization and modification, making it suitable for the development of novel materials and pharmaceuticals.
Used in Material Science:
In the field of material science, 2H-1,4-Benzoxazine, 3,4-dihydro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)can be utilized as a component in the development of advanced materials with unique properties. Its incorporation into polymers or other materials may lead to enhanced performance characteristics, such as improved thermal stability, mechanical strength, or specific chemical reactivity.
Used in Pharmaceutical Industry:
2H-1,4-Benzoxazine, 3,4-dihydro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)may have potential applications in the pharmaceutical industry as a precursor for the synthesis of new drugs or drug delivery systems. Its unique structure and the boron-containing group can be exploited to design molecules with specific biological activities or to improve the pharmacokinetic properties of existing drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 1155264-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,5,2,6 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1155264-46:
(9*1)+(8*1)+(7*5)+(6*5)+(5*2)+(4*6)+(3*4)+(2*4)+(1*6)=142
142 % 10 = 2
So 1155264-46-2 is a valid CAS Registry Number.

1155264-46-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H62290)  3,4-Dihydro-2H-1,4-benzoxazine-6-boronic acid pinacol ester   

  • 1155264-46-2

  • 250mg

  • 1474.0CNY

  • Detail
  • Alfa Aesar

  • (H62290)  3,4-Dihydro-2H-1,4-benzoxazine-6-boronic acid pinacol ester   

  • 1155264-46-2

  • 1g

  • 4388.0CNY

  • Detail

1155264-46-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydro-2H-1,4-benzoxazine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1155264-46-2 SDS

1155264-46-2Relevant academic research and scientific papers

SINGLE MOLECULE COMPOUNDS PROVIDING MULTI-TARGET INHIBITION OF BTK AND OTHER PROTEINS AND METHODS OF USE THEREOF

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Paragraph 0179; 0197, (2020/02/16)

The invention relates to compounds useful for inhibiting BTK and at least one other protein and to methods of treating diseases including cancer by administration of a compound(s) of Formula I-IV or pharmaceutically acceptable salts thereof as defined her

SYK INHIBITORS

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Paragraph 3283; 3285-3287, (2016/10/07)

The present disclosure a Syk compound inhibitors, including state cancer and inflammation and various disease States thereof in the treatment of relates to the use of. In one aspect a particular embodiment, . given by formula I which is marked as a chemical structure of compound. In formula said, X 1, X 2, X 3, R 2, R 3, R 4, R 5, and Y has described herein is. The present disclosure of a formula I compounds or a pharmaceutically acceptable salt of pharmaceutical compositions including, mediated by Syk and to treat conditions a employing these compounds and compositions further provides a method. (by machine translation)

Burton's tyrosine kinase inhibitor

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, (2017/01/17)

The invention provides a Burton's tyrosine kinase inhibitor. Particularly, a compound capable of serving as the Btk inhibitor is obtained through a wide and thorough research. It is shown through experimental results that the compound has a good inhibitin

MK2 INHIBITORS AND USES THEREOF

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, (2014/10/03)

The present invention provides compounds, compositions thereof, and methods of using the same.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

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, (2010/12/01)

Compounds of formula I wherein a, R1, R2, R3, R4, R5 and R6 are defined herein, are useful as inhibitors of HIV replication.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

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Page/Page column 112, (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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