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CAS

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14300-15-3

2'-(2-Oxopropyl)acetanilide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 14300-15-3 Structure

  • Basic information

    1. Product Name: 2'-(2-Oxopropyl)acetanilide
    2. Synonyms: 2'-(2-Oxopropyl)acetanilide;N-[2-(2-Oxopropyl)phenyl]acetamide
    3. CAS NO:14300-15-3
    4. Molecular Formula: C11H13NO2
    5. Molecular Weight: 191.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 14300-15-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 376.4±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.131±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.89±0.70(Predicted)
    10. CAS DataBase Reference: 2'-(2-Oxopropyl)acetanilide(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2'-(2-Oxopropyl)acetanilide(14300-15-3)
    12. EPA Substance Registry System: 2'-(2-Oxopropyl)acetanilide(14300-15-3)

  • 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: 14300-15-3(Hazardous Substances Data)

14300-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14300-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,0 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14300-15:
(7*1)+(6*4)+(5*3)+(4*0)+(3*0)+(2*1)+(1*5)=53
53 % 10 = 3
So 14300-15-3 is a valid CAS Registry Number.

14300-15-3SDS

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-(2-(2-oxopropyl)phenyl)acetamide

1.2 Other means of identification

Product number -
Other names N-[2-(2-Oxo-propyl)-phenyl]-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:14300-15-3 SDS

14300-15-3Downstream Products

14300-15-3Relevant articles and documents

Intramolecular cooperative C-C bond cleavage reaction of 1,3-dicarbonyl compounds with 2-iodoanilines to give o-(N-Acylamino)aryl ketones and multisubstituted indoles

Xing, Qi,Lv, Hui,Xia, Chungu,Li, Fuwei

, p. 8591 - 8596 (2015/06/02)

A copper-catalyzed C-C bond cleavage reaction of 1,3-dicarbonyl compounds with 2-iodoanilines was developed. In this process, the ortho effect played an important role in the reactivity and a new reaction pathway that involved a (2-aminophenyl)-bis-(1,3-dicarbonyl) copper species was clearly observed by a time-course HRMS analysis of the reaction mixture. Unlike the previous reports, both the nucleophilic and electrophilic parts of the 1,3-dicarbonyl compound were coupled with 2-iodoaniline by C-C bond cleavage to form o-(N-acylamino)aryl ketones, which could be efficiently converted into multisubstituted indoles.

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