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4-[(4-METHYLPHENYL)THIO]-3-NITROBENZALDEHYDE is a chemical compound characterized by its molecular formula C14H11NO3S. It is a yellow crystalline solid that features a benzene ring with a thiophenyl and nitro group attached, along with an aldehyde functional group. 4-[(4-METHYLPHENYL)THIO]-3-NITROBENZALDEHYDE is widely recognized for its applications in organic synthesis, medicinal chemistry research, and as a reagent in the preparation of various organic compounds. Its potential pharmaceutical properties and its role as a potent enzyme inhibitor make it a significant entity in biochemistry and pharmacology research.

270262-89-0

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270262-89-0 Usage

Uses

Used in Organic Synthesis:
4-[(4-METHYLPHENYL)THIO]-3-NITROBENZALDEHYDE is used as a reagent for the preparation of various organic compounds, leveraging its unique chemical structure to facilitate reactions and syntheses in the field of organic chemistry.
Used in Medicinal Chemistry Research:
In the realm of medicinal chemistry, 4-[(4-METHYLPHENYL)THIO]-3-NITROBENZALDEHYDE is utilized for its potential pharmaceutical properties, contributing to the development of new drugs and therapeutic agents.
Used in Biochemistry and Pharmacology Research:
As a potent inhibitor of certain enzymes, 4-[(4-METHYLPHENYL)THIO]-3-NITROBENZALDEHYDE is employed in biochemistry and pharmacology research to study enzyme functions and interactions, which is crucial for understanding disease mechanisms and developing targeted treatments.
Used in Pharmaceutical Development:
4-[(4-METHYLPHENYL)THIO]-3-NITROBENZALDEHYDE is used as a key intermediate in the synthesis of pharmaceuticals, particularly those targeting specific enzyme pathways, due to its ability to modulate enzyme activity and potentially treat related diseases.
Used in Chemical Research and Development:
In the chemical industry, 4-[(4-METHYLPHENYL)THIO]-3-NITROBENZALDEHYDE is used as a research tool to explore new chemical reactions and develop innovative synthetic methods, further expanding the horizons of chemical science.

Check Digit Verification of cas no

The CAS Registry Mumber 270262-89-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,0,2,6 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 270262-89:
(8*2)+(7*7)+(6*0)+(5*2)+(4*6)+(3*2)+(2*8)+(1*9)=130
130 % 10 = 0
So 270262-89-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H11NO3S/c1-10-2-5-12(6-3-10)19-14-7-4-11(9-16)8-13(14)15(17)18/h2-9H,1H3

270262-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-methylphenyl)sulfanyl-3-nitrobenzaldehyde

1.2 Other means of identification

Product number -
Other names 4-[(4-methylphenyl)sulfanyl]-3-nitrobenzaldehyde

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:270262-89-0 SDS

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