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2-Propanone, 1-(1-oxopropoxy)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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72845-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72845-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,4 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72845-79:
(7*7)+(6*2)+(5*8)+(4*4)+(3*5)+(2*7)+(1*9)=155
155 % 10 = 5
So 72845-79-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O3/c1-3-6(8)9-4-5(2)7/h3-4H2,1-2H3

72845-79-5SDS

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 2-oxopropyl propanoate

1.2 Other means of identification

Product number -
Other names propionyloxy-acetone

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:72845-79-5 SDS

72845-79-5Downstream Products

72845-79-5Relevant academic research and scientific papers

1,2-Dibromoethane and KI mediated α-acyloxylation of ketones with carboxylic acids

Wang, Xujie,Li, Gangsheng,Yang, Yanan,Jiang, Jianshuang,Feng, Ziming,Zhang, Peicheng

supporting information, p. 711 - 714 (2019/09/30)

The 1,2-dibromoethane- and KI-mediated α-acyloxylation of ketones is reported in moderate to good yield without the use of transition metals and strong oxidants. Various acids are well tolerated with wide functional group compatibility. An 1,2-dibromoethane- and KI-catalysed reaction mechanism is proposed based on the results of control experiments.

Regio- and chemoselective rearrangement of terminal epoxides into methyl alkyl and aryl ketones

Tian, Yingying,Jürgens, Eva,Kunz, Doris

supporting information, p. 11340 - 11343 (2018/10/31)

The development of the highly active pincer-type rhodium catalyst 2 for the nucleophilic Meinwald rearrangement of functionalised terminal epoxides into methyl ketones under mild conditions is presented. An excellent regio- and chemoselectivity is obtained for the first time for aryl oxiranes.

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