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N-(3-Bromo-5-ethylphenyl)acetamide, also known as Ethyl 3-bromo-5-aminobenzoate, is a chemical compound belonging to the class of acetamides. It is distinguished by the presence of a bromine atom, an ethyl group, and a phenyl group in its molecular structure, which contributes to its unique chemical properties and potential applications in various fields.

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  • 123158-67-8 Structure
  • Basic information

    1. Product Name: N-(3-BroMo-5-ethylphenyl)acetaMide
    2. Synonyms: N-(3-BroMo-5-ethylphenyl)acetaMide
    3. CAS NO:123158-67-8
    4. Molecular Formula: C10H12BrNO
    5. Molecular Weight: 242.11238
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123158-67-8.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.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(3-BroMo-5-ethylphenyl)acetaMide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(3-BroMo-5-ethylphenyl)acetaMide(123158-67-8)
    11. EPA Substance Registry System: N-(3-BroMo-5-ethylphenyl)acetaMide(123158-67-8)
  • 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: 123158-67-8(Hazardous Substances Data)

123158-67-8 Usage

Uses

Used in Organic Synthesis:
N-(3-Bromo-5-ethylphenyl)acetamide is utilized as a key intermediate in various organic synthesis reactions. Its unique structure allows it to participate in a range of chemical transformations, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, N-(3-Bromo-5-ethylphenyl)acetamide serves as a crucial building block for the development of new drugs. Its structural features enable it to be modified and optimized for specific therapeutic targets, contributing to the discovery of novel pharmaceutical agents.
Used in Medicinal Chemistry:
N-(3-Bromo-5-ethylphenyl)acetamide has potential applications in the field of medicinal chemistry, where it can be employed for the design and synthesis of bioactive compounds. Its presence of a bromine atom and other functional groups allows for the exploration of its interactions with biological targets, potentially leading to the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 123158-67-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,1,5 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 123158-67:
(8*1)+(7*2)+(6*3)+(5*1)+(4*5)+(3*8)+(2*6)+(1*7)=108
108 % 10 = 8
So 123158-67-8 is a valid CAS Registry Number.

123158-67-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid-(3-ethyl-5-bromo-anilide)

1.2 Other means of identification

Product number -
Other names Essigsaeure-(3-aethyl-5-brom-anilid)

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:123158-67-8 SDS

123158-67-8Downstream Products

123158-67-8Relevant articles and documents

Kynurenic acid derivatives useful in the treatment of neurodegenerative disorders

-

, (2008/06/13)

4-Oxo-1,4-dihydroquinoline compounds having a 2-acidic group or a group convertible thereto in vivo, and their pharmaceutically acceptable salts, are potent specific antagonists of N-methyl-D-aspartate (NMDA) receptors and are therefore useful in the treatment of neurodegenerative disorders. 4-Oxo-1,4-dihydroquinoline compounds having a 2-acidic group or a group convertible thereto in vivo, other than carboxy or C 1-6 alkoxycarbonyl, are novel compounds, as also are compounds of formula II STR1 wherein R 2 represents carboxy or a group convertible thereto in vivo, R 6 is hydrogen and R 5 and R 7 represent C 1-6 alkyl or halogen, provided that R 5 and R 7 are not simultaneously chlorine or simultaneously bromine; a process for preparing the novel compounds is described, as also are pharmaceutical compositions containing the novel compounds.

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