1698-25-5

Basic information

• Product Name: 1-DIPHENYLMETHYL-4-NITROSOPIPERAZINE
• Synonyms: 1-DIPHENYLMETHYL-4-NITROSOPIPERAZINE
• CAS NO: 1698-25-5
• Molecular Formula: C₁₇H₁₉N₃O
• Molecular Weight: 281.35
• Mol File: 1698-25-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 430.5°Cat760mmHg
• Flash Point: 214.1°C
• Appearance: /
• Density: 1.15g/cm³
• Vapor Pressure: 1.29E-07mmHg at 25°C
• Refractive Index: 1.613
• CAS DataBase Reference: 1-DIPHENYLMETHYL-4-NITROSOPIPERAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-DIPHENYLMETHYL-4-NITROSOPIPERAZINE(1698-25-5)
• EPA Substance Registry System: 1-DIPHENYLMETHYL-4-NITROSOPIPERAZINE(1698-25-5)

Safety Data

• Hazardous Substances Data: 1698-25-5(Hazardous Substances Data)

Usage

Nitrosamine derivative

A derivative of nitrosamines, which are known environmental contaminants with potential carcinogenic effects.

Potential health risks

Possibility of forming adducts with DNA, leading to DNA damage and mutagenesis.

Laboratory use

Commonly used in research and laboratory settings for its ability to form adducts with DNA.

Safety protocols

It is important to handle this chemical with caution and follow proper safety protocols in a laboratory setting.

InChI:InChI=1/C17H19N3O/c21-18-20-13-11-19(12-14-20)17(15-7-3-1-4-8-15)16-9-5-2-6-10-16/h1-10,17H,11-14H2

Upstream product

• 841-77-0 diphenylmethylpiperazine 

Relevant articles and documents

An efficient synthesis of: N -nitrosamines under solvent, metal and acid free conditions using tert -butyl nitrite

Synthesis of various N-nitroso compounds from secondary amines is reported using tert-butyl nitrite (TBN) under solvent free conditions. Broad substrate scope, metal and acid free conditions, easy isolation procedure and excellent yields are few important features of this methodology. The acid labile protecting groups such as tert-butyldimethylsilyl (TBDMS) and tert-butyloxycarbonyl (Boc) as well as sensitive functional groups such as phenols, olefins and alkynes are found to be stable under the standard reaction conditions. Besides N-nitrosation, TBN is also found to be an efficient reagent in few other transformations including aryl hydrazines to aryl azides and primary amides to carboxylic acids under mild conditions.