Welcome to LookChem.com Sign In|Join Free

CAS

  • or

131179-72-1

N-(4-Fluorophenyl)-2-(4-hydroxyphenyl)acetamide is a synthetic organic compound characterized by the presence of amide, aromatic, and halogen elements in its chemical structure. It has a molecular formula of C14H12FNO2 and is primarily defined by fluorophenyl and hydroxyphenyl groups attached to an acetamide backbone. N-(4-FLUOROPHENYL)-2-(4-HYDROXYPHENYL)ACETAMIDE does not have widespread public exposure in commercial or household products.

131179-72-1 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 131179-72-1 Structure

  • Basic information

    1. Product Name: N-(4-FLUOROPHENYL)-2-(4-HYDROXYPHENYL)ACETAMIDE
    2. Synonyms: N-(4-FLUOROPHENYL)-2-(4-HYDROXYPHENYL)ACETAMIDE
    3. CAS NO:131179-72-1
    4. Molecular Formula: C14H12FNO2
    5. Molecular Weight: 245.25
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131179-72-1.mol

  • Chemical Properties

    1. Melting Point: 139-141°C
    2. Boiling Point: 488.1°Cat760mmHg
    3. Flash Point: 249°C
    4. Appearance: /
    5. Density: 1.319g/cm3
    6. Vapor Pressure: 3.77E-10mmHg at 25°C
    7. Refractive Index: 1.639
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N-(4-FLUOROPHENYL)-2-(4-HYDROXYPHENYL)ACETAMIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-(4-FLUOROPHENYL)-2-(4-HYDROXYPHENYL)ACETAMIDE(131179-72-1)
    12. EPA Substance Registry System: N-(4-FLUOROPHENYL)-2-(4-HYDROXYPHENYL)ACETAMIDE(131179-72-1)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 131179-72-1(Hazardous Substances Data)

131179-72-1 Usage

Uses

Used in Scientific Research:
N-(4-Fluorophenyl)-2-(4-hydroxyphenyl)acetamide is used as a reference compound in scientific research for understanding the properties and reactivity of similar compounds. Its role in this context is to provide insights into the behavior of molecules with similar structural features.
Used as a Synthetic Intermediate:
In the field of organic chemistry, N-(4-Fluorophenyl)-2-(4-hydroxyphenyl)acetamide serves as a synthetic intermediate. It is utilized in the synthesis of more complex molecules, contributing to the development of new compounds with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 131179-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,1,7 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 131179-72:
(8*1)+(7*3)+(6*1)+(5*1)+(4*7)+(3*9)+(2*7)+(1*2)=111
111 % 10 = 1
So 131179-72-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H12FNO2/c15-11-3-5-12(6-4-11)16-14(18)9-10-1-7-13(17)8-2-10/h1-8,17H,9H2,(H,16,18)

131179-72-1SDS

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 N-(4-Fluorophenyl)-2-(4-hydroxyphenyl)acetamide

1.2 Other means of identification

Product number -
Other names N-(4-FLUOROPHENYL)-2-(4-HYDROXYPHENYL)ACETAMIDE

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:131179-72-1 SDS

131179-72-1Relevant articles and documents

Allosteric Modifiers of Hemoglobin. 1. Design, Synthesis, Testing, and Structure-Allosteric Activity Relationship of Novel Hemoglobin Oxygen Affinity Decreasing Agents

Randad, Ramnarayan S.,Mahran, Mona A.,Mehanna, Ahmed S.,Abraham, Donald J.

, p. 752 - 757 (2007/10/02)

Three isomeric series of 2-(aryloxy)-2-methylpropionic acids were prepared and studied for their ability to decrease the oxygen affinity of human hemoglobin A.The isomeric aryloxy groups included 4-methyl>phenoxy, 4-(arylacetamido)phenoxy, and 4-methyl>phenoxy.A total of 20 compounds were synthesized and tested.Structure-activity relationships are presented.Several of the new compounds were found to be strong allosteric effectors of hemoglobin.The two most active compounds are 2-methyl>phenoxy>-2-methylpropionic acid and the corresponding 3,5-dimethyl derivative.The latter two compounds have been compared to other known potent allosteric effectors in the same assay and show greater activity.Both compounds also exhibit a right shift in the oxygen equilibrium curve when incubated with whole blood.The new compounds may be of interest in clinical or biological areas that require or would benefit from a reversal of depleted oxygen supply (i.e., ischemia, stroke, tumor radiotherapy, blood storage, blood substitutes, etc.).They are also structurally related to several marketed antilipidemic agents.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 131179-72-1