38170-02-4

Basic information

• Product Name: 2-HYDROXY-4-IODO-BENZALDEHYDE
• Synonyms: 2-HYDROXY-4-IODO-BENZALDEHYDE;BENZALDEHYDE, 2-HYDROXY-4-IODO-
• CAS NO: 38170-02-4
• Molecular Formula: C₇H₅IO₂
• Molecular Weight: 248.02
• Mol File: 38170-02-4.mol
• Article Data: 23

Chemical Properties

• Melting Point: 87 °C
• Boiling Point: 290.0±30.0 °C(Predicted)
• Appearance: /
• Density: 2.039±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• PKA: 7.32±0.10(Predicted)
• CAS DataBase Reference: 2-HYDROXY-4-IODO-BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-HYDROXY-4-IODO-BENZALDEHYDE(38170-02-4)
• EPA Substance Registry System: 2-HYDROXY-4-IODO-BENZALDEHYDE(38170-02-4)

Safety Data

• Hazardous Substances Data: 38170-02-4(Hazardous Substances Data)

Usage

Uses

2-hydroxy-4-iodobenzaldehyde is used in the preparation of anti-B7-H3 antibodies.

Upstream product

• 67-66-3 chloroform 
• 626-02-8 3-Iodophenol 
• 75-25-2 Bromoform 
• 50-00-0 formaldehyd 
• 533-58-4 2-Iodophenol 
• 18179-39-0 methyl 4-iodosalicylate 
• 166386-81-8 2-Hydroxy-4-iodo-benzylalcohol 

Downstream Products

• 856076-61-4 2-hydroxy-4-iodo-5-nitrobenzaldehyde 
• 16870-28-3 4-iodosalicylic acid 
• 843646-60-6 (2,4-dichloro-phenyl)-(6-iodo-benzofuran-2-yl)-methanone 
• 1005238-04-9 C₂₄H₁₄O₄ 
• 1005238-05-0 C₂₃H₁₃NO₄ 
• 854028-52-7 2-benzyloxy-4-iodobenzaldehyde 
• 924708-48-5 4-iodo-2-ethenylphenol 
• 1089681-88-8 C₁₁H₉IO₃ 
• 1118519-87-1 4-(2-thienyl)salicylaldehyde 
• 1227268-30-5 2-(allyloxy)-4-iodobenzaldehyde 
• 1300036-84-3 C₃₂H₂₆BF₂IN₂O₅ 
• 1300036-85-4 C₃₇H₃₅BF₂N₂O₅Si 
• 1300036-86-5 C₃₃H₂₅BF₂N₂O₅ 
• 1300026-62-3 C₁₀H₉IO₄ 

Relevant articles and documents

A two-photon fluorescent probe for real-time monitoring of autophagy by ultrasensitive detection of the change in lysosomal polarity

The first two-photon probe, Lyso-OC, was proposed for use in monitoring cell autophagy by detection of the change in the lysosomal polarity during the membrane fusion process of autophagy. The Lyso-OC probe exhibited desirable optical properties and a det

Breathing Room: Restoring Free Rotation in a Schiff-Base Macrocycle through Endoperoxide Formation

Macrocyclization is a popular method for preparing hosts, but it can have unintended effects, like limiting molecular free rotation to yield mixtures of inseparable isomers. We report a [3 + 3] Schiff-base macrocycle (1) with anthracene bridges. Restricte

Fluorescent 7-Substituted Coumarin Dyes: Solvatochromism and NLO Studies

The effect of three substituents N,N-diethylamine, carbazole and diphenylamine at the 7 position of coumarin on linear and nonlinear optical properties are studied using absorption and emission solvatochromism, and DFT. By varying the substituent 53?nm red shift is achieved in emission. The polarity plots with regression close to unity revealed good charge transfer in the system. Solvent polarizability and dipolarity are mainly responsible for solvatochromic shift as proved by multilinear regression analysis. General Mulliken Hush analysis shows diphenylamine substituent leads to more charge separation in compound 6c. The hyperpolarizabilities are evaluated by quantum mechanical calculations. Structure of the compounds are optimized at B3LYP/6-31G(d) level and NLO computations are done using range separated hybrid functionals with large basis sets. Second order hyperpolarizability (γ) found 589.27 × 10?36, 841.29 × 10?36 and 1043.00 × 10?36 e.s.u for the compounds 6a, 6b and 6c respectively.