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N-[4-(3-OXO-PROPYL)-PHENYL]-ACETAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 169054-06-2 Structure
  • Basic information

    1. Product Name: N-[4-(3-OXO-PROPYL)-PHENYL]-ACETAMIDE
    2. Synonyms: N-[4-(3-OXO-PROPYL)-PHENYL]-ACETAMIDE;AcetaMide, N-[4-(3-oxopropyl)phenyl]-
    3. CAS NO:169054-06-2
    4. Molecular Formula: C11H13NO2
    5. Molecular Weight: 191.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 169054-06-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 382.489°C at 760 mmHg
    3. Flash Point: 165.453°C
    4. Appearance: /
    5. Density: 1.13g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.562
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 15.04±0.70(Predicted)
    11. CAS DataBase Reference: N-[4-(3-OXO-PROPYL)-PHENYL]-ACETAMIDE(CAS DataBase Reference)
    12. NIST Chemistry Reference: N-[4-(3-OXO-PROPYL)-PHENYL]-ACETAMIDE(169054-06-2)
    13. EPA Substance Registry System: N-[4-(3-OXO-PROPYL)-PHENYL]-ACETAMIDE(169054-06-2)
  • 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: 169054-06-2(Hazardous Substances Data)

169054-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169054-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,0,5 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 169054-06:
(8*1)+(7*6)+(6*9)+(5*0)+(4*5)+(3*4)+(2*0)+(1*6)=142
142 % 10 = 2
So 169054-06-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO2/c1-9(14)12-11-6-4-10(5-7-11)3-2-8-13/h4-8H,2-3H2,1H3,(H,12,14)

169054-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-(3-oxopropyl)phenyl]acetamide

1.2 Other means of identification

Product number -
Other names 4-(3'-oxoprop-1'-yl)acetanilide

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:169054-06-2 SDS

169054-06-2Relevant articles and documents

Nornicotine-organocatalyzed aqueous reduction of α,β-unsaturated aldehydes

Brogan, Andrew P.,Dickerson, Tobin J.,Janda, Kim D.

, p. 4952 - 4954 (2008/09/17)

Nornicotine, a native component of tobacco and minor nicotine metabolite, was found to catalyze the chemoselective reduction of α,β-unsaturated aldehydes under homogeneous aqueous conditions. The Royal Society of Chemistry.

7-PHENYL-ISOQUINOLINE-5-SULFONYLAMINO DERIVATIVES AS INHIBITORS OF AKT (PROTEINKINASE B)

-

Page/Page column 28, (2010/02/12)

The present invention relates to compounds Formula (I) as inhibitors of AKT activity, which are useful for the treatment of susceptible neoplasms and viral infections.

Copying nature's mechanism for the decarboxylation of β-keto acids into catalytic antibodies by reactive immunization

Bj?rnestedt, Robert,Zhong, Guofu,Lerner, Richard A.,Barbas III, Carlos F.

, p. 11720 - 11724 (2007/10/03)

Reactive immunization was used to generate catalytic antibodies that use the enamine mechanism common to the natural class I aldolase enzymes. In order to investigate the possibility of exploiting the imine and enamine intermediates programmed into antibo

Catalytic, Enantioselective Aldol Reaction with an Artificial Aldolase Assembled from a Primary Amine and an Antibody

Reymond, Jean-Louis,Chen, Yuanwei

, p. 6970 - 6979 (2007/10/03)

The aldol addition of acetone to aldehydes 1-5 is catalyzed by primary amine 14.The pH profile is consistent with catalysis by the free amine, with pKa=8.55 for its conjugate acid.The catalytic cycle involves rate-determining coupling of the aldehyde with enamine III formed by condensation of the amine and acetone.Condensation with the aldehyde to form imine 16 inhibits catalysis (k16=7.8 mM).Assembly of amine 14 with an antibody against quaternary ammonium hapten 19 yields an artificial aldolase which catalyzes the reaction.The catalyst is approximately 600 times more reactive than amine 14 alone.The pKa of the amino group is unged within the complex.The antibody catalyzes the formation of amino nitrile 17 in the presence of cyanide, suggesting that condensation of acetone with amine 14 is favored by complexation with the antibody, an effect which might account for catalysis.The reaction with aldehyde 1 is si enantioface selective and gives aldol (SS)-6 (>95percent de) from (S)-1 and aldol (RS)-6 from (R)-1 (65percent de) in 1:2.8 ratio.These experiments show the principles of a novel approach for the design of an artificial aldolase.

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