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CAS

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379254-83-8

2-chloro-N-(2-fluoro-5-nitrophenyl)acetaMide is a chemical compound with the molecular formula C8H6ClFN2O3. It is a white to off-white solid that is commonly used as an intermediate in the synthesis of pharmaceutical drugs. 2-chloro-N-(2-fluoro-5-nitrophenyl)acetaMide is known for its antibacterial and antifungal properties, making it a useful component in the development of medications.
Used in Pharmaceutical Industry:
2-chloro-N-(2-fluoro-5-nitrophenyl)acetaMide is used as an intermediate in the synthesis of pharmaceutical drugs for its antibacterial and antifungal properties, contributing to the development of antibiotics and antimicrobial agents.
It is important to handle 2-chloro-N-(2-fluoro-5-nitrophenyl)acetaMide with care as it may be harmful if ingested, inhaled, or comes into contact with the skin.

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  • 379254-83-8 Structure

  • Basic information

    1. Product Name: 2-chloro-N-(2-fluoro-5-nitrophenyl)acetaMide
    2. Synonyms: 2-chloro-N-(2-fluoro-5-nitrophenyl)acetaMide;AcetaMide, 2-chloro-N-(2-fluoro-5-nitrophenyl)-
    3. CAS NO:379254-83-8
    4. Molecular Formula: C8H6ClFN2O3
    5. Molecular Weight: 232.5962432
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 379254-83-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-chloro-N-(2-fluoro-5-nitrophenyl)acetaMide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-chloro-N-(2-fluoro-5-nitrophenyl)acetaMide(379254-83-8)
    11. EPA Substance Registry System: 2-chloro-N-(2-fluoro-5-nitrophenyl)acetaMide(379254-83-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 379254-83-8(Hazardous Substances Data)

379254-83-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 379254-83-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,9,2,5 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 379254-83:
(8*3)+(7*7)+(6*9)+(5*2)+(4*5)+(3*4)+(2*8)+(1*3)=188
188 % 10 = 8
So 379254-83-8 is a valid CAS Registry Number.

379254-83-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-N-(2-fluoro-5-nitrophenyl)acetamide

1.2 Other means of identification

Product number -
Other names T0511-4785

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:379254-83-8 SDS

379254-83-8Relevant articles and documents

SMALL MOLECULE STING ANTAGONISTS

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Page/Page column 177-178, (2021/08/20)

The present invention relates to compounds of formula (I). The compounds maybe used to antagonise the Stimulator of Interferon Genes (STING) protein and may thereby treat liver fibrosis, fatty liver disease, non-alcoholic steatohepatitis (NASH), pulmonary fibrosis, lupus, sepsis, rheumatoid arthritis (RA), type I diabetes, STING- associated vasculopathy with onset in infancy (SAVI), Aicardi-Goutieres syndrome (AGS), familial chilblain lupus (FCL), systemic lupus erythematosus (SLE), retinal vasculopathy, neuroinflammation, systemic inflammatory response syndrome, pancreatitis, cardiovascular disease, renal fibrosis, stroke and age-related macular degeneration (AMD).

Synthesis of quinoxaline derivatives from substituted acetanilides through intramolecular quaternization reactions

De Castro, Sonia,Chicharro, Roberto,Aran, Vicente J.

, p. 790 - 802 (2007/10/03)

The cyclization of 2-dialkylamino-2′-halogeno- and 2-chloro-2′-(dialkylamino)acetanilides to quinoxaline derivatives has been studied in detail. These reactions proceed, respectively, through intramolecular aromatic nucleophilic or aliphatic nucleophilic

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