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2,4-Pentadienenitrile,5-(dimethylamino)-,(2E,4E)-(9CI), also known as dimethylamino-4-[(2E,4E)-pentadien-2-yl]benzonitrile, is a chemical compound with the molecular formula C9H11N3. It is a clear, colorless liquid that is highly reactive and should be handled with caution due to its potential toxicity and environmental impact.

77226-56-3

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77226-56-3 Usage

Uses

Used in Pharmaceutical Industry:
2,4-Pentadienenitrile,5-(dimethylamino)-,(2E,4E)-(9CI) is used as a chemical intermediate in the manufacture of pharmaceuticals. Its unique chemical structure allows it to be incorporated into the synthesis of various organic compounds, contributing to the development of new drugs and therapeutic agents.
Used in Organic Compounds Production:
2,4-Pentadienenitrile,5-(dimethylamino)-,(2E,4E)-(9CI) is used as a key ingredient in the production of organic compounds. Its reactivity and versatility make it a valuable component in the synthesis of a wide range of organic molecules, including dyes, insecticides, and other specialty chemicals.
Used in Dyes Industry:
2,4-Pentadienenitrile,5-(dimethylamino)-,(2E,4E)-(9CI) is used as a chemical intermediate in the production of dyes. Its ability to form stable complexes with other molecules makes it an essential component in the creation of vibrant and long-lasting colorants for various applications.
Used in Insecticides Industry:
2,4-Pentadienenitrile,5-(dimethylamino)-,(2E,4E)-(9CI) is also used in the production of insecticides. Its reactivity and potential to form stable complexes with other molecules make it a valuable component in the development of effective and long-lasting insect control agents.
Used in Organic Synthesis:
2,4-Pentadienenitrile,5-(dimethylamino)-,(2E,4E)-(9CI) has potential applications in the field of organic synthesis. Its unique chemical properties and reactivity make it a promising candidate for the synthesis of complex organic molecules and the development of new chemical reactions.
Used in Medicinal Chemistry:
2,4-Pentadienenitrile,5-(dimethylamino)-,(2E,4E)-(9CI) also has potential applications in medicinal chemistry. Its ability to form stable complexes with other molecules and its reactivity make it a valuable tool in the design and synthesis of new pharmaceutical agents and drug candidates.

Check Digit Verification of cas no

The CAS Registry Mumber 77226-56-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,2 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 77226-56:
(7*7)+(6*7)+(5*2)+(4*2)+(3*6)+(2*5)+(1*6)=143
143 % 10 = 3
So 77226-56-3 is a valid CAS Registry Number.

77226-56-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E,4E)-5-Dimethylamino-penta-2,4-dienenitrile

1.2 Other means of identification

Product number -
Other names -

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:77226-56-3 SDS

77226-56-3Downstream Products

77226-56-3Relevant academic research and scientific papers

DERIVATIVES AND REACTIONS OF GLUTACONALDEHYDE-XII. PHOTOCHEMICAL AND THERMAL PREPERATION OF 5-AMINO-2,4-PENTADIENENITRILES

Becher, J.,Finsen, L.,Winckelmann, I.,Koganty, R. Rao,Buchardt, O.

, p. 789 - 793 (2007/10/02)

Irradiation of pyridine N-oxide (1) in the presence of secondary amines in aqueous solution produces mixtures of isomric 2Z,4E and N,N-disubstituted all-E 5-amino-2,4-pentadienenitriles (3 and 4), in fair yields, and with an ease to render the reaction preparatively useful.Furthermore, such compounds can be prepared thermally by dehydration of 5-amino-2,4-pentadienal oximes.

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