147-58-0

Basic information

• Product Name: 2'-IODOHIPPURIC ACID
• Synonyms: o-Iodohippuric Acid (100 mg);o-Iodohippuric acid for synthesis;2'-IODOHIPPURIC ACID;2-IODOHIPPURIC ACID;(2-IODOBENZOYL)GLYCINE;O-IODOHIPPURIC ACID;N-(2-IODOBENZOYL)GLYCINE;Glycine,N-(2-iodobenzoyl)-
• CAS NO: 147-58-0
• Molecular Formula: C₉H₈INO₃
• Molecular Weight: 305.07
• EINECS: 205-693-5
• Mol File: 147-58-0.mol
• Article Data: 1

Chemical Properties

• Melting Point: 170-172 °C(lit.)
• Boiling Point: 480.9 °C at 760 mmHg
• Flash Point: 244.6 °C
• Appearance: /
• Density: 1.871 g/cm³
• Vapor Pressure: 4.67E-10mmHg at 25°C
• Refractive Index: 1.643
• Storage Temp.: Store below +30°C.
• Solubility: DMSO (Slightly), Methanol (Slightly)
• BRN: 1877943
• CAS DataBase Reference: 2'-IODOHIPPURIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2'-IODOHIPPURIC ACID(147-58-0)
• EPA Substance Registry System: 2'-IODOHIPPURIC ACID(147-58-0)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• Hazardous Substances Data: 147-58-0(Hazardous Substances Data)

Usage

Uses

o-Iodohippuric Acid is used as a probe to measure renal function and clearance.

InChI:InChI=1/C9H8INO3/c10-7-4-2-1-3-6(7)9(14)11-5-8(12)13/h1-4H,5H2,(H,11,14)(H,12,13)

Upstream product

• 69238-60-4 N-(methoxycarbonylmethyl)-2-iodobenzamide 
• 609-67-6 2-Iodobenzoyl chloride 
• 88-67-5 2-Iodobenzoic acid 
• 56-40-6 glycine 

Downstream Products

• 100731-12-2 [CuI(2,2'-bipyridine)2]I 
• 88-67-5 2-Iodobenzoic acid 
• 56-40-6 glycine 

Relevant articles and documents

Metal-free synthesis of 3,3-disubstituted oxoindoles by iodine(III)-catalyzed bromocarbocyclizations

"I" did it: An iodine(III)-mediated bromocarbocyclization was elaborated as an efficient tool for the synthesis of oxoindoles. This method is applicable to a variety of structurally different substrates, also with chemically sensitive groups, and gives access to the heterocycles in a regio- and stereoselective fashion (see scheme). The indole-2-ones obtained can be converted easily into structurally complex target compounds, such as the alkaloid physostigmine. Copyright