91335-51-2

Basic information

• Product Name: 2-BROMO-4,5-DIETHOXYBENZALDEHYDE
• Synonyms: AN-655/15531053;MLS000770730;SMR000343893;STK045225;ZINC00336070
• CAS NO: 91335-51-2
• Molecular Formula: C₁₁H₁₃BrO₃
• Molecular Weight: 273.13
• Mol File: 91335-51-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 343.6 °C at 760 mmHg
• Flash Point: 161.6 °C
• Appearance: /
• Density: 1.377 g/cm³
• Vapor Pressure: 6.97E-05mmHg at 25°C
• Refractive Index: 1.551
• CAS DataBase Reference: 2-BROMO-4,5-DIETHOXYBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-4,5-DIETHOXYBENZALDEHYDE(91335-51-2)
• EPA Substance Registry System: 2-BROMO-4,5-DIETHOXYBENZALDEHYDE(91335-51-2)

Safety Data

• Hazardous Substances Data: 91335-51-2(Hazardous Substances Data)

Usage

General Description

2-Bromo-4,5-diethoxybenzaldehyde is a chemical compound with the molecular formula C11H13BrO3. It is a white to light yellow crystalline powder with a strong odor. 2-BROMO-4,5-DIETHOXYBENZALDEHYDE is commonly used in the synthesis of organic compounds and pharmaceutical intermediates. It is also used as a reagent in chemical reactions and as a building block in the production of other chemicals. 2-Bromo-4,5-diethoxybenzaldehyde has potential applications in the fields of medicine, agriculture, and material science due to its unique chemical properties. However, it is important to handle this chemical with care as it may pose health and environmental risks.

InChI:InChI=1/C11H13BrO3/c1-3-14-10-5-8(7-13)9(12)6-11(10)15-4-2/h5-7H,3-4H2,1-2H3

Upstream product

• 139-85-5 3,4-dihydroxybenzaldehyde 
• 2029-94-9 3,4-diethoxybenzaldehyde 

Downstream Products

• 1351800-58-2 2-(1,3-dioxolan-2-yl)-4,5-diethoxybenzonitrile 
• 1351800-60-6 4,5-diethoxy-2-formylbenzonitrile 
• 1351800-57-1 2-(2-bromo-4,5-diethoxyphenyl)-1,3-dioxolane 
• 1186310-03-1 bis-1,4-(tert-butyldimethylsiloxymethyl)-bis-2,5-(2'-formyl-4',5'-diethoxyphenyl-ethynyl)benzene 

Relevant articles and documents

Exquisite synthesis of a designed PAR-1 antagonist

The synthesis of a designed, sterically congested geminal dimethyl-bearing PAR-1 antagonist was achieved by a route of ten steps, with the oxidation of an electron-rich benzaldehyde, the construction of a tertiary alkyl azide, and the selective hydrogenolysis of a 1,5-fused tetrazole to generate the cyclic amidine with Raney-Ni being the key steps. The selective hydrogenolysis of 1,5-fused tetrazole to generate the cyclic amidine with Raney-Ni was discovered and may be generally used for the synthesis of structurally unusual cyclic amidines. Several unsuccessful attempts to construct the desired geminal dimethyl-bearing cyclic amidine were also discussed. Copyright