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9-Ethylcarbazole-3-carboxaldehyde N-benzyl-N-phenylhydrazone is a hydrazone derivative of the carbazole compound, featuring an ethyl group and a phenyl group. It is a chemical compound used in various organic synthesis reactions and chemical research. Its unique structure and functional groups make it a valuable reagent in organic chemistry, and its potential biological activities, including antioxidant and anticancer properties, make it an interesting target for further research in medicinal and materials science.

75238-79-8

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75238-79-8 Usage

Uses

Used in Organic Synthesis:
9-Ethylcarbazole-3-carboxaldehyde N-benzyl-N-phenylhydrazone is used as a reagent in various organic synthesis reactions due to its unique structure and functional groups, contributing to the development of new chemical compounds.
Used in Chemical Research:
9-ETHYLCARBAZOLE-3-CARBOXALDEHYDE N-BENZYL-N-PHENYLHYDRAZONE is utilized in chemical research to explore its potential applications and properties, such as its ability to scavenge free radicals and inhibit oxidative stress, making it a promising candidate for further study in medicinal and materials science.
Used in Antioxidant Applications:
9-Ethylcarbazole-3-carboxaldehyde N-benzyl-N-phenylhydrazone exhibits potential antioxidant properties, making it a candidate for use in applications that require protection against oxidative stress and free radical damage.
Used in Anticancer Applications:
9-ETHYLCARBAZOLE-3-CARBOXALDEHYDE N-BENZYL-N-PHENYLHYDRAZONE has been found to exhibit potential anticancer properties, suggesting its use in the development of new therapeutic agents for cancer treatment.
Used in Fluorescent Materials Development:
9-Ethylcarbazole-3-carboxaldehyde N-benzyl-N-phenylhydrazone is used in the development of fluorescent materials, taking advantage of its unique optical properties for various applications, such as sensors, imaging, and diagnostics.
Used in Pharmaceutical Compounds Synthesis:
9-ETHYLCARBAZOLE-3-CARBOXALDEHYDE N-BENZYL-N-PHENYLHYDRAZONE serves as a building block in the synthesis of pharmaceutical compounds, leveraging its potential biological activities and unique structure to create new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 75238-79-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,3 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75238-79:
(7*7)+(6*5)+(5*2)+(4*3)+(3*8)+(2*7)+(1*9)=148
148 % 10 = 8
So 75238-79-8 is a valid CAS Registry Number.
InChI:InChI=1/C28H25N3/c1-2-30-27-16-10-9-15-25(27)26-19-23(17-18-28(26)30)20-29-31(24-13-7-4-8-14-24)21-22-11-5-3-6-12-22/h3-20H,2,21H2,1H3

75238-79-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-Ethyl-3-(N-benzyl-N-phenylhydrazonomethyl)carbazole

1.2 Other means of identification

Product number -
Other names 9-ETHYLCARBAZOLE-3-CARBOXALDEHYDE N-BENZYL-N-PHENYLHYDRAZONE

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:75238-79-8 SDS

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