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14556-98-0

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14556-98-0 Usage

Description

4-Chloro-2-hydroxy-5-sulfamoylbenzoic acid, also known as 4-chloro salicylic acid-5-sulfonamide, is an aryl sulfonamide derivative characterized by its white solid appearance. It is a chemical compound with a unique structure that features a chlorine atom at the 4th position, a hydroxyl group at the 2nd position, and a sulfamoyl group at the 5th position of the benzene ring. 4-Chloro-2-hydroxy-5-sulfamoylbenzoic acid is known for its potential applications in various industries due to its chemical properties.

Uses

Used in Pharmaceutical Industry:
4-Chloro-2-hydroxy-5-sulfamoylbenzoic acid is used as an intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of drugs targeting specific medical conditions. Its unique chemical structure allows it to serve as a building block for creating new and effective medications.
Used in Chemical Synthesis:
In the field of chemical synthesis, 4-Chloro-2-hydroxy-5-sulfamoylbenzoic acid is utilized as a key intermediate for the production of a wide range of chemical compounds. Its versatility in reacting with other molecules makes it a valuable component in the synthesis of various organic compounds, including those with potential applications in different industries.
Used in Research and Development:
4-Chloro-2-hydroxy-5-sulfamoylbenzoic acid is also used in research and development laboratories for studying its chemical properties and potential applications. Scientists and researchers can use this compound to explore new reaction pathways, develop novel synthetic methods, and investigate its potential as a precursor to other valuable chemicals.
Used in Xipamide Production:
Specifically, 4-Chloro-2-hydroxy-5-sulfamoylbenzoic acid is used as an intermediate in the production of Xipamide, a medication used for treating conditions related to fluid and electrolyte balance in the body. Its role in the synthesis of Xipamide highlights its importance in the pharmaceutical industry and its contribution to the development of life-saving drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 14556-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,5 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14556-98:
(7*1)+(6*4)+(5*5)+(4*5)+(3*6)+(2*9)+(1*8)=120
120 % 10 = 0
So 14556-98-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClNO5S/c8-4-2-5(10)3(7(11)12)1-6(4)15(9,13)14/h1-2,10H,(H,11,12)(H2,9,13,14)

14556-98-0 Well-known Company Product Price

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  • Aldrich

  • (545805)  4-Chloro-2-hydroxy-5-sulfamoylbenzoicacid  96%

  • 14556-98-0

  • 545805-25G

  • 4,124.25CNY

  • Detail

14556-98-0SDS

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 4-Chloro-2-Hydroxy-5-Sulfamoylbenzoic Acid

1.2 Other means of identification

Product number -
Other names 4-Chloro-5-sulfamoyl-salicylic Acid

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:14556-98-0 SDS

14556-98-0Relevant articles and documents

Study of the structure of Besulpamide, 1-[(4-Chloro-3-sulfamoylbenzoyl)amino]-2,4,6-trimethylpyridinium hydroxide inner salt, and related compounds, using X-ray crystallography and 1H and 13C nuclear magnetic resonance spectroscopy

Frigola

, p. 1373 - 1382 (2007/10/02)

The diuretic and antihypertensive drug Besulpamide, 1-[(4-Chloro-3-sulfamoylbenzoyl)amino]-2,4,6-trimethylpyridinium hydroxide inner salt, and related compounds have been investigated by nmr spectroscopy and mass spectrometry. A mechanism for the formation of the salt 5 is proposed. The tautomerism of hydroxy derivatives of Besulpamide is discussed on the basis of nmr spectroscopy. The single-crystal X-ray investigation of Besulpamide, R = 0.038 (Rw = 0.041), showed two crystallographically independent molecular conformations in the crystal structure, space group PI, a = 8.485(3), b = 14.282(2), c = 15.312(6), α = 69.41(2), β = 82.22(4), γ = 72.78(3).

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