6647-96-7

Basic information

• Product Name: MFCD15146432
• Synonyms: 1H-Pyrazole, 4-iodo-1,5-dimethyl-
• CAS NO: 6647-96-7
• Molecular Formula: C₅H₇IN₂
• Molecular Weight: 222.03
• Mol File: 6647-96-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: MFCD15146432(CAS DataBase Reference)
• NIST Chemistry Reference: MFCD15146432(6647-96-7)
• EPA Substance Registry System: MFCD15146432(6647-96-7)

Safety Data

• Hazardous Substances Data: 6647-96-7(Hazardous Substances Data)

Usage

General Description

MFCD15146432 is a chemical compound identified with the chemical name of 2-oxo-2-phenylethyl nitrate. It has a molecular formula of C8H7NO4 and a molecular weight of 177.15 g/mol. MFCD15146432 is a nitrate ester and is commonly used as a reagent in organic synthesis reactions. It is a colorless to pale yellow liquid with a characteristic odor and is known to be sensitive to heat, light, and air. MFCD15146432 is also classified as a hazardous substance and should be handled with care, as it is potentially explosive.

Upstream product

• 39806-90-1 4-iodo-1-methyl-1H-pyrazole 
• 74-88-4 methyl iodide 
• 694-31-5 1,5-dimethyl-1H-pyrazole 
• 1453-58-3 3-Methylpyrazole 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 71443-54-4 1,5-dimethyl-4-phenylethynyl-1H-pyrazole 
• 3920-42-1 1,5-dimethyl-4-nitro-1H-pyrazole 
• 75092-30-7 4-iodo-1-methyl-1H-pyrazole-5-carboxylic acid 

Relevant articles and documents

2 - Alkynyl mannose derivative and application thereof

The present invention relates to a 2-alkynyl mannose derivative and an application thereof. The mannose derivative, as well as a pharmaceutically acceptable salt, an isotope and an isomer thereof have the structure represented by general formula I. The de

Two-stage sonogashira coupling method in the synthesis of auxin active acetylenes

A sequential Sonogashira coupling of a protected acetylene precursor with aryl halides (5) followed by pyrazolyl iodides (14) allows efficient access to the unsymmetrical aryl-heteroarylacetylene (8). Subsequent regioselective lithiation exchange followed by dimethyl oxalate quench produced readily vicinal ketoesters (9) which show auxin effects in a wide variety of plant species.