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(1E)-1-pyridin-4-ylethanone N-4-[(E)-phenyldiazenyl]phenylsemicarbazone is a complex organic chemical compound characterized by a pyridine ring connected to an ethanone group and a semicarbazone moiety attached to a phenyldiazenyl group. As a semicarbazone derivative, it incorporates azo and carbonyl functional groups, which contribute to its potential applications in organic synthesis and medicinal chemistry. Due to its intricate molecular structure and associated safety concerns, it is essential to handle (1E)-1-pyridin-4-ylethanone N-{4-[(E)-phenyldiazenyl]phenyl}semicarbazone with care.

7598-87-0

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7598-87-0 Usage

Uses

Used in Organic Synthesis:
(1E)-1-pyridin-4-ylethanone N-4-[(E)-phenyldiazenyl]phenylsemicarbazone is utilized as a key intermediate in organic synthesis for the development of new compounds with potential applications across various industries. Its unique structure allows for the creation of a wide range of derivatives, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (1E)-1-pyridin-4-ylethanone N-4-[(E)-phenyldiazenyl]phenylsemicarbazone serves as a precursor for the synthesis of bioactive molecules. Its semicarbazone and phenyldiazenyl moieties can be leveraged to design and develop novel therapeutic agents with potential applications in treating various diseases and medical conditions. (1E)-1-pyridin-4-ylethanone N-4-[(E)-phenyldiazenyl]phenylsemicarbazone's versatility in chemical modifications makes it an attractive candidate for drug discovery and optimization processes.
Used in Research and Development:
(1E)-1-pyridin-4-ylethanone N-4-[(E)-phenyldiazenyl]phenylsemicarbazone is also employed in research and development settings to explore its chemical properties and reactivity. Scientists and chemists use (1E)-1-pyridin-4-ylethanone N-{4-[(E)-phenyldiazenyl]phenyl}semicarbazone to study reaction mechanisms, investigate its interactions with other molecules, and understand its potential role in various chemical and biological processes. This research can lead to new insights and advancements in the fields of chemistry and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 7598-87-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7598-87:
(6*7)+(5*5)+(4*9)+(3*8)+(2*8)+(1*7)=150
150 % 10 = 0
So 7598-87-0 is a valid CAS Registry Number.

7598-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-phenyldiazenylphenyl)-3-[(E)-1-pyridin-4-ylethylideneamino]urea

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 -
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More Details:7598-87-0 SDS

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