136545-11-4

Basic information

• Product Name: 2,2-DiMethyl-6-nitro-3,4-dihydro-2H-1,4-benzoxazine, 97%
• Synonyms: 2,2-DiMethyl-6-nitro-3,4-dihydro-2H-1,4-benzoxazine, 97%;2,2-Dimethyl-6-nitro-3,4-dihydro-2H-benzo[b][1,4]oxazine;2,2-dimethyl-6-nitro-3,4-dihydro-1,4-benzoxazine
• CAS NO: 136545-11-4
• Molecular Formula: C₁₀H₁₂N₂O₃
• Molecular Weight: 208.21388
• Mol File: 136545-11-4.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,2-DiMethyl-6-nitro-3,4-dihydro-2H-1,4-benzoxazine, 97%(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-DiMethyl-6-nitro-3,4-dihydro-2H-1,4-benzoxazine, 97%(136545-11-4)
• EPA Substance Registry System: 2,2-DiMethyl-6-nitro-3,4-dihydro-2H-1,4-benzoxazine, 97%(136545-11-4)

Safety Data

• Hazard Codes: T
• Statements: 25
• Safety Statements: 45
• RIDADR: UN 2811 6.1 / PGIII
• Hazardous Substances Data: 136545-11-4(Hazardous Substances Data)

Usage

Purity

97% pure

Chemical structure

Dihydrobenzoxazine ring with two methyl groups (-CH3) and a nitrogen atom

Functional group

Nitro group (-NO2)

Type of compound

Benzoxazine derivative

Potential applications

Pharmaceutical, agrochemical, or materials industries

Usage

Research and development, or as a starting material for the synthesis of other compounds

Safety precautions

Handle with care, may have hazardous properties, and should be used in a controlled laboratory setting.

Upstream product

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• 85160-84-5 3,4-dihydro-2,2-dimethyl-6-nitro-3-oxo-2H-1,4-benzoxazine 

Downstream Products

• 136544-11-1 2-(3,4-dihydro-2,2-dimethyl-6-nitro-2H-1,4-benzoxazin-4-yl)pyridine N-oxide 
• 174714-67-1 2,2-Dimethyl-6-nitro-4-pyridin-3-ylmethyl-3,4-dihydro-2H-benzo[1,4]oxazine 
• 174714-66-0 3,4-dihydro-2,2-dimethyl-6-nitro-4-(pyridin-2-ylmethyl)-2H-1,4-benzoxazine 

Relevant articles and documents

MK2 INHIBITORS AND USES THEREOF

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

SUBSTITUTED ARYL-AMINE DERIVATIVES AND METHODS OF USE

The present invention provides classes of compounds, including-their pharmaceutically acceptable derivatives, useful for treating angiogenesis and related diseases such as cancer. Formula I and II wherein R is a 9- or 10-membered heterocyclyl ring selected from 7-isoquinolinyl,..2-methyl-3-oxo-2,3-dihydroindazol-6-yl, [1,6]-naphthydrin-3-yl, [1,7]-naphthydrin-2-yl, 1-oxo-2,3-dihydrobenzofuran-4-yl, 3-oxo-2,3-dihydrobenzofuran-5-yl, dihydro-benzodioxinyl, 6-quinazolinyl, 2-amino-6-quinazolinyl, 4-methylamino-6-quinazolinyl, 2,4-diamino-6 quinazolinyl, 3-oxo-3,4-dihydro-1,4-benzoxazin-6-yl, 2,2-difluoro-l;3-benzodioxol-5-yl and 2,2,3,3 tetrafluoro-2,3-dihydro-l,4-benzodioxin-6-yl, each of which is optionally substituted with one or more substituents selected from halo, haloakyl, C1-6 alkyl, C2-8 alkenyl, C2-8 alkynyl, N-dimethylamino-C1-6-alkyl, N-dimethylamino-C1-6-alkoxy, amino, alkyl-carbonylamino, morpholino-sulfonyl, amino-sulfonyl, oxazolyl, pyrrolyl,4 morpholinyl, carboxyl, cyano, and acetyl; wherein R1 in formula I is selected from unsubstituted or substituted phenyl, 5-6 membered heteroaryl, 9-10 membered bicyclic heterocyclyl and 11-14 membered tricyclic heterocyclyl, and R1 in formula II is selected from specific bicyclic heterocycles.

Substituted alkylamine derivatives and methods of use

Selected amines are effective for prophylaxis and treatment of diseases, such as angiogenesis mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.