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2-Propanone,1-[(2-aminobenzoyl)oxy]-(9CI), also known as 2-propoxybenzoylacetanilide, is a chemical compound with the molecular formula C11H13NO3. It belongs to the class of organic compounds known as phenylpropanoic acids and is a derivative of acetophenone. Its molecular structure consists of a benzoyl group attached to a propanone moiety. 2-Propanone,1-[(2-aminobenzoyl)oxy]-(9CI) has potential biological activity and may have applications in medicinal chemistry and drug development.

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  • 130627-09-7 Structure
  • Basic information

    1. Product Name: 2-Propanone,1-[(2-aminobenzoyl)oxy]-(9CI)
    2. Synonyms: 2-Propanone,1-[(2-aminobenzoyl)oxy]-(9CI);2-Oxopropyl 2-aMinobenzoate
    3. CAS NO:130627-09-7
    4. Molecular Formula: C10H11NO3
    5. Molecular Weight: 193.2
    6. EINECS: N/A
    7. Product Categories: AMINOACID
    8. Mol File: 130627-09-7.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.: 2-8°C(protect from light)
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Propanone,1-[(2-aminobenzoyl)oxy]-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Propanone,1-[(2-aminobenzoyl)oxy]-(9CI)(130627-09-7)
    11. EPA Substance Registry System: 2-Propanone,1-[(2-aminobenzoyl)oxy]-(9CI)(130627-09-7)
  • 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: 130627-09-7(Hazardous Substances Data)

130627-09-7 Usage

Uses

Used in Pharmaceutical Industry:
2-Propanone,1-[(2-aminobenzoyl)oxy]-(9CI) is used as an intermediate in the production of various pharmaceuticals. Its unique molecular structure allows it to be a key component in the synthesis of drugs with specific therapeutic properties.
Used in Organic Synthesis:
2-Propanone,1-[(2-aminobenzoyl)oxy]-(9CI) is used as a reagent in organic synthesis. Its versatile chemical properties enable it to be a valuable building block in the creation of complex organic molecules for various applications.
Used in Medicinal Chemistry and Drug Development:
Due to its potential biological activity, 2-Propanone,1-[(2-aminobenzoyl)oxy]-(9CI) may have applications in medicinal chemistry and drug development. Researchers can explore its interactions with biological targets and evaluate its potential as a lead compound for the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 130627-09-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,2 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 130627-09:
(8*1)+(7*3)+(6*0)+(5*6)+(4*2)+(3*7)+(2*0)+(1*9)=97
97 % 10 = 7
So 130627-09-7 is a valid CAS Registry Number.

130627-09-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Anthranilsaeureacetonylester

1.2 Other means of identification

Product number -
Other names 2-oxopropyl 2-aminobenzoate

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:130627-09-7 SDS

130627-09-7Relevant articles and documents

Structural analogues of quinoline alkaloids: Straightforward route to [1,3]dioxolo[4,5-c]quinolines with antibacterial properties

?am?ulová, Veronika,Funk, Petr,Grepl, Martin,Horák, Radim,Hradil, Pavel,Ko?istek, Kamil,Kvapil, Lubomír,Slaninová, Ludmila,Soural, Miroslav

, (2020)

Compounds bearing [1,3]dioxolo-quinoline scaffolds have been found in quinoline-based natural products; the only exception is the [1,3]dioxolo[4,5-c]quinoline moiety with a rare occurrence in both natural and synthetic derivatives. In this article, we report the preparation of diversely substituted and functionalized [1,3]dioxolo[4,5-c]quinolines using [1,3]dioxolo[4,5-c]quinoline-4-carbaldehyde (DQC) as the common intermediate. DQC was synthesized on a large scale from anthranilic acid and chloroacetone as the starting materials, with the rearrangement of acetonyl-anthranilate as the key step. The developed method allows for the simple preparation of [1,3]dioxolo[4,5-c]quinolines with various C2 substituents on the quinoline scaffold. Additionally, the synthetic route was successfully applied to the preparation of 3-hydroxyquinoline-4(1H)-ones. The target compounds were tested against representative Gram-positive/negative bacteria, and two derivatives exhibited submicromolar minimum inhibitory concentrations against Micrococcus luteus.

Preparation of 1,2-disubstituted-3-hydroxy-4(1H)-quinolinones and the influence of substitution on the course of cyclization

Hradil, Pavel,Hlavac, Jan,Lemr, Karel

, p. 141 - 144 (2007/10/03)

Synthesis of 1,2-disubstituted-3-hydroxy-4(1H)-quinolinones by the cyclization of N-substituted phenacyl or acetonyl anthranilates is described. Two methods were employed for cyclization of anthranilates. Heating in polyphosphoric acid has a wide scope of applicability. The thermal cyclization in boiling N-methylpyrrolidone is limited by steric effect.

Synthesis of 2-Substituted 1H-Benzoxazepin-5-ones

Sicker, Dieter

, p. 336 - 344 (2007/10/02)

An approach to the hitherto unknown class of 1H-benz>e>oxazepin-5-ones is given based on reduction and cyclization of appropriate acyclic ortho-nitro compounds as starting material.Thus, some 2-substituted derivatives (3a-i) were synthesized by catal

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