138505-25-6

Basic information

• Product Name: 5-BROMO-2-ISOPROPOXYBENZALDEHYDE
• Synonyms: 5-BROMO-2-ISOPROPOXYBENZALDEHYDE;5-Bromo-2-(1-methylethoxy)benzaldehyde;5-bromo-2-propan-2-yloxybenzaldehyde;5-bromo-2-propan-2-yloxy-benzaldehyde
• CAS NO: 138505-25-6
• Molecular Formula: C₁₀H₁₁BrO₂
• Molecular Weight: 243.11
• Mol File: 138505-25-6.mol
• Article Data: 17

Chemical Properties

• Melting Point: 31-33 °C
• Boiling Point: 309.7±22.0 °C(Predicted)
• Appearance: /
• Density: 1.391±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 5-BROMO-2-ISOPROPOXYBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMO-2-ISOPROPOXYBENZALDEHYDE(138505-25-6)
• EPA Substance Registry System: 5-BROMO-2-ISOPROPOXYBENZALDEHYDE(138505-25-6)

Safety Data

• Hazardous Substances Data: 138505-25-6(Hazardous Substances Data)

Usage

General Description

5-Bromo-2-isopropoxybenzaldehyde is an organic compound, belonging to the family of bromobenzenes. Its chemical formula is C10H11BrO2. This chemical, like other bromobenzenes, features a bromine atom attached to a benzene ring, making it a halogenated aromatic compound. Additionally, it possesses an aldehyde functional group and an isopropoxy group. The presence of the bromine atom allows this substance to act as a good leaving group in organic reactions. While the aldehyde group lends it to be reactive, the isopropoxy group enhances its solubility in organic solvents. Specific information about its toxicity and handling precautions may vary, so material safety data sheets (MSDS) should always be consulted while handling this chemical.

Upstream product

• 515832-52-7 5-bromo-2-[(1-methylethyl)oxy]benzonitrile 
• 40530-18-5 5-bromo-2-hydroxybenzonitrile 
• 22921-58-0 2-isopropoxybenzaldehyde 
• 75-30-9 2-iodo-propane 
• 1761-61-1 5-bromosalicyclaldehyde 
• 75-26-3 isopropyl bromide 

Downstream Products

• 1210502-10-5 C₁₃H₁₄N₂O₂ 
• 1210502-11-6 C₁₅H₁₅NO₂ 
• 1296134-48-9 iPrMgCl 
• 138505-26-7 5-Bromo-2-isopropoxyphenol 
• 1180496-52-9 ethyl phenyl-{4-(isopropoxy)-3-vinylphenyl}phosphinate 
• 1180496-53-0 ethyl (4-fluorophenyl)-[4-{isopropoxy}-3-vinylphenyl]-phosphinate 
• 1173178-94-3 C₁₅H₁₇BrO₅ 

Relevant articles and documents

Tris(perfluoroalkyl)silyl entities as unexpectedly potent tags for the noncovalent immobilization of catalysts by fluorous-fluorous interactions: Application to the synthesis of several perfluoro-tagged ligands

Unexpectedly high retention times were obtained in HPLC investigations for compounds equipped with (C8F17CH2CH 2)3Si tags on C8F17-modified silica gel (Fig. 4). Hence, these tags have a high potential for the noncovalent immobilization of catalysts to be applied in organic solvents, allowing for an easy separation and reuse of the catalyst by filtration and reapplication. The tris(perfluoroalkyl)silyl tag could be incorporated in a straightforward manner into ligands as demonstrated by the synthesis of several prominent classes of ligands (Schemes 4-6).

S1P1 AGONIST AND APPLICATION THEREOF

The present invention relates to a class of tricyclic compounds and an application thereof as a sphingosine 1-phosphate type 1 (S1P1) receptor agonist. The invention specifically relates to a compound represented by formula (II), and a tautomer and pharmaceutically acceptable salt of same.

Phosphinate ruthenium complexes

Provided herein are ruthenium complexes of Formula I, and processes of preparation thereof. Also provided are methods of their use as a metathesis catalyst.