66739-89-7

Basic information

• Product Name: 2-(4-CYANOPHENYL)-1 3-DIOXOLANE
• Synonyms: RARECHEM AL BP 0074;2-(4-CYANOPHENYL)-1 3-DIOXOLANE;4-(1,3-DIOXOLAN-2-YL)BENZONITRILE
• CAS NO: 66739-89-7
• Molecular Formula: C₁₀H₉NO₂
• Molecular Weight: 175.18
• Mol File: 66739-89-7.mol
• Article Data: 55

Chemical Properties

• Boiling Point: 317.6°C at 760 mmHg
• Flash Point: 132.8°C
• Appearance: /
• Density: 1.21g/cm³
• Vapor Pressure: 0.00038mmHg at 25°C
• Refractive Index: 1.562
• CAS DataBase Reference: 2-(4-CYANOPHENYL)-1 3-DIOXOLANE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-CYANOPHENYL)-1 3-DIOXOLANE(66739-89-7)
• EPA Substance Registry System: 2-(4-CYANOPHENYL)-1 3-DIOXOLANE(66739-89-7)

Safety Data

• HazardClass: 6.1
• Hazardous Substances Data: 66739-89-7(Hazardous Substances Data)

Usage

General Description

2-(4-cyanophenyl)-1,3-dioxolane is an organic compound with the molecular formula C10H7NO2. It is a colorless liquid with a slightly sweet odor that is commonly used as a pharmaceutical intermediate in the synthesis of various drugs. This chemical is also used as a solvent in the production of perfumes and as a reagent in organic chemistry. It is primarily known for its ability to form a stable and soluble complex with metal ions, making it useful in the extraction and separation of metal ions from various solutions. Additionally, 2-(4-cyanophenyl)-1,3-dioxolane has been studied for its potential applications in the field of polymer chemistry due to its unique structure and reactivity.

InChI:InChI=1/C10H9NO2/c11-7-8-1-3-9(4-2-8)10-12-5-6-13-10/h1-4,10H,5-6H2

Upstream product

• 107-21-1 ethylene glycol 
• 105-07-7 4-cyanobenzaldehyde 
• 646-06-0 1,3-DIOXOLANE 
• 623-03-0 4-Cyanochlorobenzene 
• 623-00-7 4-bromobenzenecarbonitrile 
• 3058-39-7 4-iodobenzonitrile 
• 630-18-2 tert-butyl isocyanide 
• 10602-01-4 p-bromobenzaldehyde 1,3-dioxolane 
• 1663-39-4 tert-Butyl acrylate 

Downstream Products

• 444169-52-2 2-hydroxyethyl 4-cyanobenzoate 
• 868280-61-9 1-[4-(1,3-dioxolan-2-yl)phenyl]-2-phenylethanone 
• 480390-48-5 5-[4-(1,3-dioxolan-2-yl)phenyl]-1H-tetrazole 
• 1240309-56-1 1-(4-(1,3-dioxolan-2-yl)phenyl)-2-(3-(trifluoromethyl)phenyl)ethanone 
• 1240309-67-4 1-(4-(1,3-dioxolan-2-yl)phenyl)hexan-1-one 
• 1233933-12-4 N-[4-(1,3-dioxacyclopent-2-yl)benzyl]octanamide 
• 950491-35-7 N-(4-formylbenzyl)octanamide 
• 1354638-40-6 α-(4-butanamidomethyl)phenyl-N-(2-hydroxymethyl-1,3-dihydroxy-2-propyl)nitrone 
• 1354638-41-7 α-(4-hexanamidomethyl)phenyl-N-(2-hydroxymethyl-1,3-dihydroxy-2-propyl)nitrone 
• 1354638-42-8 α-(4-octanamidomethyl)phenyl-N-(2-hydroxymethyl-1,3-dihydroxy-2-propyl)nitrone 
• 1354638-43-9 α-(4-decanamidomethyl)phenyl-N-(2-hydroxymethyl-1,3-dihydroxy-2-propyl)nitrone 
• 1354638-45-1 C₁₆H₂₃N₂O₅ 
• 1354638-46-2 C₁₈H₂₇N₂O₅ 
• 1354638-47-3 C₂₀H₃₁N₂O₅ 

Relevant articles and documents

A nitroolefin functionalized DPP fluorescent probe for the selective detection of hydrogen sulfide

In this paper, a nitroolefin functionalized probe DPP-NO2 was designed and synthesized as a selective fluorescent probe for detection of hydrogen sulfide (H2S). The specific reduction reaction between the nitro group and H2/sub

Porosity-induced emission: exploring color-controllable fluorescence of porous organic polymers and their chemical sensing applications

Most organic dyes dissipate their excitation energy in the aggregated state because of the "aggregation-caused quenching" effect, deteriorating their application in optoelectronic devices. To prevent the "aggregation-caused quenching" effect, we incorpora

A colorimetric probe based on diketopyrrolopyrrole and tert-butyl cyanoacetate for cyanide detection

A new colorimetric probe 1 comprising a diketopyrrolopyrrole-based Michael receptor, which recognized cyanide anions with high selectivity, was designed and synthesized. Addition of CN- aqueous solution to 1 in THF resulted in a rapid color cha

Photochemical C-H Activation Enables Nickel-Catalyzed Olefin Dicarbofunctionalization

Alkenes, ethers, and alcohols account for a significant percentage of bulk reagents available to the chemistry community. The petrochemical, pharmaceutical, and agrochemical industries each consume gigagrams of these materials as fuels and solvents each year. However, the utilization of such materials as building blocks for the construction of complex small molecules is limited by the necessity of prefunctionalization to achieve chemoselective reactivity. Herein, we report the implementation of efficient, sustainable, diaryl ketone hydrogen-atom transfer (HAT) catalysis to activate native C-H bonds for multicomponent dicarbofunctionalization of alkenes. The ability to forge new carbon-carbon bonds between reagents typically viewed as commodity solvents provides a new, more atom-economic outlook for organic synthesis. Through detailed experimental and computational investigation, the critical effect of hydrogen bonding on the reactivity of this transformation was uncovered.

Ester compound based on pyrrolopyrrolediketone and having solid-liquid double fluorescence and application

The invention discloses an ester compound based on pyrrolopyrrolediketone and having solid-liquid double fluorescence, which has the following structural general formula; wherein the R1, R2, R3, R4 and R5 are respectively and independently selected from h

Pyrrole-pyrroledione-based derivative fluorescent probe and application thereof

The invention discloses a pyrrole-pyrrole-dione-based derivative as shown in the formula I. R Is selected from - CH. 3 . - (CH)2 )n CH3 , (CH)2 )m CH2 X, CH (CH)3 )su