29949-16-4

Basic information

• Product Name: 2,2-diphenylpentanenitrile
• CAS NO: 29949-16-4
• Molecular Formula: C₁₇H₁₇N
• Molecular Weight: 235.3236
• Mol File: 29949-16-4.mol

Chemical Properties

• Boiling Point: 354.4°C at 760 mmHg
• Flash Point: 172.9°C
• Density: 1.027g/cm³
• Vapor Pressure: 3.35E-05mmHg at 25°C
• Refractive Index: 1.555
• CAS DataBase Reference: 2,2-diphenylpentanenitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-diphenylpentanenitrile(29949-16-4)
• EPA Substance Registry System: 2,2-diphenylpentanenitrile(29949-16-4)

Safety Data

• Hazardous Substances Data: 29949-16-4(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
2,2-diphenylpentanenitrile is used as a key intermediate in organic synthesis for its strong electron-withdrawing properties, facilitating various chemical reactions and contributing to the formation of a wide range of organic compounds.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 2,2-diphenylpentanenitrile is utilized as a building block for the synthesis of diverse pharmaceuticals. Its unique molecular structure allows for the creation of new drug candidates with potential therapeutic applications.
Used in Agrochemical Production:
2,2-diphenylpentanenitrile also finds application in the agrochemical sector, where it serves as a precursor for the development of various agrochemicals, including pesticides and herbicides, due to its reactivity and structural properties.
Used in Chemical Research:
As a potentially hazardous chemical with a strong odor, 2,2-diphenylpentanenitrile is employed in chemical research to study its properties and reactions, contributing to the advancement of chemical knowledge and the discovery of new applications.

Upstream product

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Downstream Products

• 719-79-9 1,1-diphenylbutane 
• 841-32-7 SKF 2314 
• 108971-43-3 2,2′-diphenyl-aminopentane 
• 101583-99-7 2,2-diphenyl-valeric acid amide 
• 13080-07-4 2,2-diphenyl-valeryl chloride 
• 302-33-0 proadifen 
• 7475-84-5 N-(2,2-diphenyl-pentyl)-benzamide 
• 7500-29-0 N-(2,2-diphenyl-pentyl)-N'-phenyl-thiourea 
• 854458-55-2 1,1-bis-(4-nitro-phenyl)-butane 
• 40691-84-7 (2,2-diphenyl-pentyl)-carbamic acid ethyl ester 
• 25347-16-4 2,2-diphenyl-valeric acid-(2-dimethylamino-ethyl ester); hydrochloride 

Relevant articles and documents

Chiral lanthanide complexes: Coordination chemistry, spectroscopy, and catalysis

The coordination chemistry and catalytic applications of organometallic and related lanthanide complexes bearing chiral oxazoline ligands is an area that has been largely underdeveloped, in comparison to complexes based upon lanthanide triflates for use i

Molecular Modification of Anticholinergics as Probes for Muscarinic Receptors. Amino Esters of α-Substituted Phenylacetic Acid and Related Analogues

Two series of compounds having the general structure of C6H5CRR'COOCH2CH2NEt2 were synthesized and examined for their antispasmodic activities.These compounds were selected as structural probes for exploring the nature of muscarinic cholinergic receptor binding sites that interact with atropine-like anticholinergics.These studies indicate a rather strict size limitation for the hydrophobic region of the receptor and suggest intramolecular hydrogen bonding as a possible means to explain the observed stereoselectivity.