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3-Cyano-5-nitrobenzoic acid is a chemical compound with a molecular formula of C8H4N2O4, characterized by its yellow crystalline solid appearance and a molecular weight of 188.13 g/mol. As a derivative of benzoic acid, it features both a cyano group and a nitro group, which contribute to its utility as a building block in the synthesis of a variety of organic compounds.

98556-65-1

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98556-65-1 Usage

Uses

Used in Pharmaceutical Industry:
3-Cyano-5-nitrobenzoic acid is used as a key intermediate for the synthesis of various pharmaceuticals, given its ability to be incorporated into complex organic molecules that can exhibit therapeutic properties.
Used in Dye Industry:
3-CYANO-5-NITROBENZOIC ACID is utilized as a precursor in the production of dyes, where its chemical structure can contribute to the color and stability of the final dye products.
Used in Organic Chemicals Manufacturing:
3-Cyano-5-nitrobenzoic acid serves as a fundamental building block in the creation of other organic chemicals, playing a crucial role in the development of a wide range of chemical products.
Used in Agrochemical Production:
As an intermediate, 3-Cyano-5-nitrobenzoic acid is used in the production of agrochemicals, potentially contributing to the development of new pesticides or other agricultural products.
Used in Materials Science:
3-Cyano-5-nitrobenzoic acid has potential applications in materials science, where it can be used as a precursor for the preparation of various functional materials, highlighting its versatility in different scientific fields.

Check Digit Verification of cas no

The CAS Registry Mumber 98556-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,5,5 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 98556-65:
(7*9)+(6*8)+(5*5)+(4*5)+(3*6)+(2*6)+(1*5)=191
191 % 10 = 1
So 98556-65-1 is a valid CAS Registry Number.

98556-65-1SDS

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 3-Cyano-5-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 3-Cyan-5-nitro-benzoesaeure

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:98556-65-1 SDS

98556-65-1Relevant academic research and scientific papers

INSECTICIDAL COMPOUNDS

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Page/Page column 37, (2008/12/07)

A compound of formula (I), wherein A1, A2, A3, A4, R1, R2, R3, G1, G2, G3 and Q are as defined in claim 1; or a salt or N-oxide thereof. Furthermore, the present invention relates to processes and intermediates for preparing compounds of formula (I), to insecticidal, acaricidal, molluscicidal and nematicidal compositions comprising them and to methods of using them to combat and control insect, acarine, mollusc and nematode pests.

INSECTICIDAL COMPOUNDS

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Page/Page column 50, (2008/12/06)

A compound of formula (I): wherein A1, A2, A3, A4, R1, R2, G1, G2, Q1 and Q2 are as defined in claim 1; or a salt or N-oxide thereof. Furthermore

Heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists

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, (2008/06/13)

The present invention provides compounds and pharmaceutical compositions that act as antagonists at metabotropic glutamate receptors, and that are useful for treating neurological diseases and disorders. Methods of preparing the compounds also are disclosed.

Antibiotic compounds

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, (2008/06/13)

The present invention relates to carbapenems and provides a compound of the formula (I): STR1 or a pharmaceutically acceptable salt or in vivo hydrolysable ester thereof wherein: R1 is 1-hydroxyethyl, 1-fluoroethyl or hydroxymethyl; R2 is hydrogen or C1-4 alkyl; R3 is hydrogen or C1-4 alkyl; R4 and R5 are the same or different and are selected from hydrogen, halo, cyano, C1-4 alkyl, nitro, hydroxy, carboxy, C1-4 alkoxy, C1-4 alkoxycarbonyl, aminosulphonyl, C1-4 alkylaminosulphonyl, di-C1-4 alkylaminosulphonyl, carbamoyl, C1-4 alkylcarbamoyl, di-C1-4 alkylcarbamoyl, trifluoromethyl, sulphonic acid, amino, C1-4 alkylamino, di-C1-4 alkylamino, C1-4 alkanoylamino, C1-4 alkanoyl(N-C1-4 alkyl)amino, C1-4 alkanesulphonamido and C1-4 alkylS(O)n -- wherein n is zero, one or two: with the proviso that there is no hydroxy or carboxy substituent in a position ortho to the --NR2 --. Processes for their preparation, intermediates in their preparation, their use as therapeutic agents and pharmaceutical compositions containing them.

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