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2,4-Pentadienamide, 5-phenyl-N-(phenylmethyl)-, (2E,4E)-, also known as pentadienamide, is a chemical compound characterized by its molecular formula C17H17N and a molar mass of 235.32 g/mol. This yellow liquid with a strong odor is insoluble in water but readily soluble in organic solvents. 2,4-Pentadienamide, 5-phenyl-N-(phenylmethyl)-, (2E,4E)-'s name includes the (2E,4E)configuration, which denotes the specific geometric arrangement of its double bonds, a feature that is crucial for its chemical properties and reactivity.

142039-55-2

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142039-55-2 Usage

Uses

Used in Chemical Synthesis:
2,4-Pentadienamide, 5-phenyl-N-(phenylmethyl)-, (2E,4E)is utilized as an intermediate in the synthesis of various other chemicals. Its unique structure and reactivity make it a valuable component in the creation of a wide range of chemical products.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, 2,4-Pentadienamide, 5-phenyl-N-(phenylmethyl)-, (2E,4E)serves as a raw material for the production of certain drugs. Its specific chemical properties allow it to be incorporated into the molecular structures of pharmaceuticals, potentially contributing to their therapeutic effects.
Used in Agrochemical Production:
2,4-Pentadienamide, 5-phenyl-N-(phenylmethyl)-, (2E,4E)also finds application in the agrochemical sector, where it is used as a starting material for the development of products such as pesticides and herbicides. Its role in these applications is to provide the necessary chemical backbone for the active ingredients.
Used in Dye Manufacturing:
2,4-Pentadienamide, 5-phenyl-N-(phenylmethyl)-, (2E,4E)is employed in the dye industry to produce a variety of dyes. Its chemical structure contributes color and stability to the dyes, making it suitable for use in textiles and other coloring applications.
Used in Laboratory Research:
As a chemical reagent, 2,4-Pentadienamide, 5-phenyl-N-(phenylmethyl)-, (2E,4E)is used in laboratory research to explore its chemical properties and potential applications. Researchers leverage its reactivity to study reactions and mechanisms that could lead to new discoveries in organic chemistry.
Used in the Preparation of Synthetic Organic Compounds:
2,4-Pentadienamide, 5-phenyl-N-(phenylmethyl)-, (2E,4E)is also utilized in the preparation of synthetic organic compounds, where its unique structure and properties are harnessed to create novel materials with specific characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 142039-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,0,3 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 142039-55:
(8*1)+(7*4)+(6*2)+(5*0)+(4*3)+(3*9)+(2*5)+(1*5)=102
102 % 10 = 2
So 142039-55-2 is a valid CAS Registry Number.

142039-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-5-phenylpenta-2,4-dienamide

1.2 Other means of identification

Product number -
Other names 5-phenylpenta-2,4-dienoic acid benzyl amide

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:142039-55-2 SDS

142039-55-2Relevant academic research and scientific papers

Efficient Synthesis of Chiral α- and β-Hydroxy Amides: Application to the Synthesis of (R)-Fluoxetine

Kakei, Hiroyuki,Nemoto, Tetsuhiro,Ohshima, Takashi,Shibasaki, Masakatsu

, p. 317 - 320 (2007/10/03)

Four flavors for epoxide openings: The regioselective openings of epoxy amides obtained by asymmetric epoxidation yields all types of aryl- and alkyl-substituted hydroxy amides sometimes counter to the reactivity of the α- and β-positions.

Asymmetric synthesis of a β-lactam framework via the conjugate addition of amidocuprates(I) to chiral enoates

Asao,Uyehara,Tsukada,Yamamoto

, p. 2103 - 2111 (2007/10/03)

Amidocuprate(I) reagents {Li[Cu(NR2)2]} and higher order cyanocuprates(I) {Li2[Cu(CN)(NR2)2]} have been developed as a new class of nitrogen nucleophiles. These reagents underwent regioselective 1,4-a

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