169054-06-2

• 

• 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
  9. Article Data: 4

• 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)

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• N-[4-(3-OXO-PROPYL)-PHENYL]-ACETAMIDE

  Cas No: 169054-06-2

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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

169054-06-2Upstream product

• 221029-58-9 (E)-N-(4-(3-oxoprop-1-en-1-yl)phenyl)acetamide 
• 540-37-4 p-aminoiodobenzene 
• 622-50-4 4-Acetamido-1-iodobenzene 
• 107-18-6 allyl alcohol 

169054-06-2Downstream Products

• 169053-99-0 6-(4'-acetamidophenyl)-3-hexen-2-one 
• 221029-58-9 (E)-N-(4-(3-oxoprop-1-en-1-yl)phenyl)acetamide 
• 184001-20-5 2-Acetyl-5-(4-acetylamino-phenyl)-pentanoic acid ethyl ester 
• 184001-18-1 4-(acetamido)phenylpropyl bromide 
• 184001-14-7 N-(4-(3-hydroxypropyl)phenyl)acetamide 

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.

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

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