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142867-52-5

N-ACETYL-N-ACETOXY-4-CHLOROBENZENESULFONAMIDE is a chemical compound that belongs to the class of organic compounds known as benzenesulfonamides. These compounds are organosulfur compounds containing a benzenesulfonamide moiety, which consists of a benzenesulfonic acid moiety linked to an aniline or substituted aniline. The chemical formula of N-ACETYL-N-ACETOXY-4-CHLOROBENZENESULFONAMIDE is C10H10ClNO5S. Its detailed properties and toxicological profile have been studied, and safety precautions should be taken when handling this material.

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  • 142867-52-5 Structure

  • Basic information

    1. Product Name: N-ACETYL-N-ACETOXY-4-CHLOROBENZENESULFONAMIDE
    2. Synonyms: N,O-DIACETYL-N-HYDROXY-4-CHLOROBENZENESULFONAMIDE;N,O-DIACETYL-N-HYDROXY-4-CHLOROBENZENESULFONAMINE;O-ACETYL-N-(4-CHLOROPHENYLSULFONYL)ACETHYDROXAMIC ACID;N-ACETOXY-N-ACETYL-4-CHLOROBENZENESULFONAMIDE;N-ACETYL-N-ACETOXY-4-CHLOROBENZENESULFONAMIDE;N-ACETYL-N-ACETOXY-4-CHLOROBENZENESULPHONAMIDE;N-ACETOXY-N-ACETYL-4-CHLOROBENZENE- &;N-Acetoxy-N-(4-chlorophenylsulfonyl)acetamide
    3. CAS NO:142867-52-5
    4. Molecular Formula: C10H10ClNO5S
    5. Molecular Weight: 291.71
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 142867-52-5.mol

  • Chemical Properties

    1. Melting Point: 119-122 °C
    2. Boiling Point: 401.4 °C at 760 mmHg
    3. Flash Point: 196.6 °C
    4. Appearance: /
    5. Density: 1.454 g/cm3
    6. Vapor Pressure: 1.18E-06mmHg at 25°C
    7. Refractive Index: 1.559
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. BRN: 5821854
    11. CAS DataBase Reference: N-ACETYL-N-ACETOXY-4-CHLOROBENZENESULFONAMIDE(CAS DataBase Reference)
    12. NIST Chemistry Reference: N-ACETYL-N-ACETOXY-4-CHLOROBENZENESULFONAMIDE(142867-52-5)
    13. EPA Substance Registry System: N-ACETYL-N-ACETOXY-4-CHLOROBENZENESULFONAMIDE(142867-52-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: 22-24/25
    4. WGK Germany: 3
    5. RTECS:
    6. F: 10-21
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 142867-52-5(Hazardous Substances Data)

142867-52-5 Usage

Uses

Used in Chemical Industry:
N-ACETYL-N-ACETOXY-4-CHLOROBENZENESULFONAMIDE is used as an intermediate in the synthesis of various chemical compounds for industrial applications. Its unique structure allows it to be a key component in the production of pharmaceuticals, dyes, and other specialty chemicals.
Used in Pharmaceutical Industry:
N-ACETYL-N-ACETOXY-4-CHLOROBENZENESULFONAMIDE is used as a building block in the development of new drugs. Its chemical properties make it a valuable precursor in the synthesis of various pharmaceutical agents, contributing to the advancement of medicine and healthcare.
Used in Dye Industry:
N-ACETYL-N-ACETOXY-4-CHLOROBENZENESULFONAMIDE is used as a starting material in the production of dyes. Its chemical structure provides a foundation for the creation of a wide range of colors and hues, which are essential in various industries such as textiles, plastics, and printing.
Used in Research and Development:
N-ACETYL-N-ACETOXY-4-CHLOROBENZENESULFONAMIDE is used as a research compound in academic and industrial laboratories. Its unique properties make it an interesting subject for studies in organic chemistry, materials science, and related fields, leading to new discoveries and innovations.

Check Digit Verification of cas no

The CAS Registry Mumber 142867-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,8,6 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 142867-52:
(8*1)+(7*4)+(6*2)+(5*8)+(4*6)+(3*7)+(2*5)+(1*2)=145
145 % 10 = 5
So 142867-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H10ClNO5S/c1-7(13)12(17-8(2)14)18(15,16)10-5-3-9(11)4-6-10/h3-6H,1-2H3

142867-52-5 Well-known Company Product Price

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  • Aldrich

  • (A9584)  N-Acetoxy-N-acetyl-4-chlorobenzenesulfonamide  ≥98%

  • 142867-52-5

  • A9584-5MG

  • 985.14CNY

  • Detail

142867-52-5SDS

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 [acetyl-(4-chlorophenyl)sulfonylamino] acetate

1.2 Other means of identification

Product number -
Other names Tocris-0722

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:142867-52-5 SDS

142867-52-5Downstream Products

142867-52-5Relevant articles and documents

Optimization of HNO production from N, O - Bis -acylated hydroxylamine derivatives

Sutton, Art D.,Williamson, Morgan,Weismiller, Hilary,Toscano, John P.

supporting information; experimental part, p. 472 - 475 (2012/03/26)

A wide range of N,O-bis-acylated hydroxylamine derivatives with chloro or arenesulfonyl leaving groups, and a related set of N-hydroxy-N-acylsulfonamides, have been synthesized and evaluated for nitroxyl (HNO) production. Mechanistic studies have revealed that the observed aqueous chemistry is more complicated than originally anticipated, and have been used to develop a new series of efficient HNO precursors (4u-4x, 7c-7d) with tunable half-lives.

Bis-Acylated Hydroxylamine Derivatives

-

, (2011/06/24)

The invention provides certain bis-acylated hydroxylamine derivative compounds, pharmaceutical compositions and kits comprising such compounds, and methods of using such compounds or pharmaceutical compositions. In particular, the invention provides methods of using such compounds or pharmaceutical compositions for treating, preventing, or delaying the onset and/or develop of a disease or condition. In some embodiments, the disease or condition is selected from cardiovascular diseases, ischemia, reperfusion injury, cancerous disease, pulmonary hypertension and conditions responsive to nitroxyl therapy.

Prodrugs of Nitroxyl as Inhibitors of Aldehyde Dehydrogenase

Lee, Melinda J. C.,Nagasawa, Herbert T.,Elberling, James A.,DeMaster, Eugene G.

, p. 3648 - 3652 (2007/10/02)

In the preceding paper, analogs of chlorpropamide with an OMe substituent on the sulfonamide nitrogen were shown to inhibit aldehyde dehydrogenase (AlDH), and it was postulated that these compounds were bioactivated by O-demethylation to release nitroxyl

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