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2-Nitrobenzoic acid sodium salt, with the chemical formula C7H4NO4Na, is a sodium salt of 2-nitrobenzoic acid, a derivative of benzoic acid. It is a yellow crystalline solid that is soluble in water and has a variety of industrial and research applications.

17264-82-3

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17264-82-3 Usage

Uses

Used in Organic Synthesis:
2-Nitrobenzoic acid sodium salt is used as a reagent in organic synthesis for the preparation of various compounds.
Used in Pharmaceutical Industry:
2-Nitrobenzoic acid sodium salt is used as a reagent in the preparation of various pharmaceuticals, contributing to the development of new drugs.
Used in Agrochemical Industry:
2-Nitrobenzoic acid sodium salt is used in the preparation of agrochemicals, aiding in the development of products for agricultural applications.
Used in Dye and Pigment Manufacturing:
2-Nitrobenzoic acid sodium salt is employed in the manufacturing of dyes and pigments, playing a role in the production of colorants for various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 17264-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,6 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17264-82:
(7*1)+(6*7)+(5*2)+(4*6)+(3*4)+(2*8)+(1*2)=113
113 % 10 = 3
So 17264-82-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H5NO4.Na/c9-7(10)5-3-1-2-4-6(5)8(11)12;/h1-4H,(H,9,10);/q;+1/p-1

17264-82-3SDS

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 2-NITROBENZOIC ACID SODIUM SALT

1.2 Other means of identification

Product number -
Other names 2-NO2C6H4CO2Na

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:17264-82-3 SDS

17264-82-3Upstream product

17264-82-3Relevant academic research and scientific papers

Complex Polyheterocycles and the Stereochemical Reassignment of Pileamartine A via Aza-Heck Triggered Aryl C-H Functionalization Cascades

Bower, John F.,Caiger, Lewis,García-Cárceles, Javier,Hazelden, Ian R.,Jones, Benjamin T.,Langer, Thomas,Lewis, Richard J.

supporting information, p. 15593 - 15598 (2021/10/12)

Structurally complex benzo- and spiro-fused N-polyheterocycles can be accessed via intramolecular Pd(0)-catalyzed alkene 1,2-aminoarylation reactions. The method uses N-(pentafluorobenzoyloxy)carbamates as the initiating motif, and this allows aza-Heck-type alkene amino-palladation in advance of C-H palladation of the aromatic component. The chemistry is showcased in the first total synthesis of the complex alkaloid (+)-pileamartine A, which has resulted in the reassignment of its absolute stereochemistry.

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