51632-28-1

Basic information

• Product Name: 4-ETHYLPHENYLACETONITRILE
• Synonyms: 4-ETHYLPHENYLACETONITRILE;4-Ethylbenzyl cyanide;2-(4-Ethylphenyl)
• CAS NO: 51632-28-1
• Molecular Formula: C₁₀H₁₁N
• Molecular Weight: 145.2
• EINECS: -0
• Mol File: 51632-28-1.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 110°C 1mm
• Flash Point: 110°C/1mm
• Appearance: /
• Density: 0,97 g/cm3
• Vapor Pressure: 0.0189mmHg at 25°C
• Refractive Index: 1.5164
• Storage Temp.: 2-8°C
• BRN: 2613187
• CAS DataBase Reference: 4-ETHYLPHENYLACETONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-ETHYLPHENYLACETONITRILE(51632-28-1)
• EPA Substance Registry System: 4-ETHYLPHENYLACETONITRILE(51632-28-1)

Safety Data

• Hazard Codes: Xi
• Statements: 20/21/22
• Safety Statements: 23-36/37/39
• RIDADR: 3276
• HazardClass: 6.1
• PackingGroup: III
• Hazardous Substances Data: 51632-28-1(Hazardous Substances Data)

Usage

General Description

4-Ethylphenylacetonitrile is a chemical compound with the molecular formula C10H11N. It is an organic compound containing a nitrile functional group and an ethyl-substituted phenyl ring. It is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It is also utilized as an intermediate in the production of other organic chemicals. 4-Ethylphenylacetonitrile is known for its role as a precursor in the synthesis of various compounds, making it an important chemical for the pharmaceutical and agrochemical industries.

InChI:InChI=1/C10H11N/c1-2-9-3-5-10(6-4-9)7-8-11/h3-6H,2,7H2,1H3

Upstream product

• 143-33-9 sodium cyanide 
• 1467-05-6 4-ethylbenzylchloride 
• 57825-30-6 4-ethylbenzyl bromide 
• 768-59-2 4-ethylbenzyl alcohol 
• 16331-45-6 p-ethylbenzoyl chloride 
• 100-41-4 ethylbenzene 
• 2103-57-3 2,3,4-trimethoxybenzaldehyde 

Downstream Products

• 101096-84-8 2-(4-ethyl-phenyl)-3c-[2]furyl-acrylonitrile 
• 14387-10-1 (4-ethyl-phenyl)-acetic acid 
• 64353-29-3 4-ethylphenylethylamine 
• 109094-20-4 2-(4-ethyl-phenyl)-3c-(4-dimethylamino-phenyl)-acrylonitrile 
• 14062-20-5 ethyl (4-ethyl-phenyl)-acetate 
• 51632-19-0 4-Ethyl-α-isopropylphenylacetonitril 
• 960048-16-2 2-(4-ethylphenyl)-3-oxo-4-phenylbutanenitrile 
• 1005793-19-0 C₁₇H₁₃N₂O₂F₃ 
• 950508-65-3 2-(4-ethylphenyl)-3-phenylpropan-2-one 
• 29148-28-5 diethyl 4-ethylphenylmalonate 
• 51526-06-8 4,4'-diethyl-bibenzyl 
• 7439-15-8 1-(4-ethylphenyl)-2-phenylethane 
• 103-29-7 1,1'-(1,2-ethanediyl)bisbenzene 

Relevant articles and documents

Making a difference on excited-state chemistry by controlling free space within a nanocapsule: Photochemistry of 1-(4-alkylphenyl)-3-phenylpropan-2-ones

The free space within a reaction cavity plays a determining role during the excited-state reaction of 1-(4-alkylphenyl)-3-phenylpropan-2-ones included within a capsule formed by two molecules of a deep cavity cavitand. By controlling the free space within the reaction cavity through remote alkyl substitution on the reactant ketone it is possible to control the yield of the rearrangement product shown above.

Coumarin derivative and use thereof

The present invention provides compounds having 12-lipoxygenase inhibitory effect and medicines inhibiting 12-lipoxygenase selectively, and relates to novel coumarin derivatives and medicines containing the compounds as effective ingredients. Furthermore,

Enzymes in organic synthesis 50. Probing the dimensions of the large hydrophobic binding region of the active site of pig liver esterase using substituted aryl malonate substrates

The active side model reported recently for the synthetically useful enzyme pig liver esterase (PLE) permits the structural specificity and stereoselectivity of the enzyme to be interpreted and predicted for a wide range of substrates. The specifications