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(4-ETHOXY-PHENYL)-OXO-ACETONITRILE, with the molecular formula C10H9NO2, is a nitrile compound characterized by the presence of a phenyl group with an ethoxy substituent and an oxo group, indicating the presence of a carbonyl group. This chemical compound has potential applications in organic synthesis and pharmaceutical research, serving as a building block for more complex molecules.

62869-42-5

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62869-42-5 Usage

Uses

Used in Organic Synthesis:
(4-ETHOXY-PHENYL)-OXO-ACETONITRILE is used as a building block in organic synthesis for the creation of more complex molecules. Its unique structure allows for various chemical reactions, making it a valuable component in the synthesis of a wide range of organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (4-ETHOXY-PHENYL)-OXO-ACETONITRILE is used as a starting material for the development of new drugs. Its chemical properties and reactivity make it a promising candidate for the synthesis of pharmaceutical agents with potential therapeutic applications.
It is crucial to handle (4-ETHOXY-PHENYL)-OXO-ACETONITRILE with care and follow proper safety precautions, as nitrile compounds can be toxic and irritating if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 62869-42-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,6 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62869-42:
(7*6)+(6*2)+(5*8)+(4*6)+(3*9)+(2*4)+(1*2)=155
155 % 10 = 5
So 62869-42-5 is a valid CAS Registry Number.

62869-42-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethoxybenzoyl cyanide

1.2 Other means of identification

Product number -
Other names (4-ethoxy-phenyl)-glyoxylonitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62869-42-5 SDS

62869-42-5Relevant academic research and scientific papers

Process for the preparation of acyl cyanide compounds

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, (2008/06/13)

Acyl cyanides of the formula STR1 wherein R is alkyl or substituted alkyl with 1 to 8 carbon atoms, or cyano-carbonyl substituted alkyl, i.e., containing another STR2 group, cycloalkyl or substituted cycloalkyl with 3 to 12 carbon atoms or aryl or substituted aryl or represents an optionally substituted 5-membered or 6-membered heterocyclic radical which can additionally also be fused with a benzene ring, Are made by reacting the corresponding acid halide with an alkali metal cyanide or anhydrous hydrocyanic acid in the presence of a heavy metal cyanide and optionally in the presence of a diluent, at a temperature of between 100° C. and 300° C.

Process for the preparation of certain acyl cyanide compounds

-

, (2008/06/13)

Acyl cyanide compounds of the formula STR1 are prepared by reacting an acid halide of the formula STR2 with anhydrous hydrocyanic acid in the presence of a tertiary amine at a temperature between -70° and +100° C. R can be hydrocarbyl or substituted hydrocarbyl and X is halogen.

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