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23193-18-2

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23193-18-2 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 46, p. 4631, 1981 DOI: 10.1021/jo00335a084

Check Digit Verification of cas no

The CAS Registry Mumber 23193-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,9 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 23193-18:
(7*2)+(6*3)+(5*1)+(4*9)+(3*3)+(2*1)+(1*8)=92
92 % 10 = 2
So 23193-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O5/c1-4-14-9(12)8(6-7(3)11)10(13)15-5-2/h8H,4-6H2,1-3H3

23193-18-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-(2-oxopropyl)propanedioate

1.2 Other means of identification

Product number -
Other names Acetonyl-malonsaeure-diaethylester

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:23193-18-2 SDS

23193-18-2Relevant articles and documents

Photo-Organocatalysis of Atom-Transfer Radical Additions to Alkenes

Arceo, Elena,Montroni, Elisa,Melchiorre, Paolo

, p. 12064 - 12068 (2014)

We have found that an organic molecule as simple as p-anisaldehyde efficiently catalyzes the intermolecular atom-transfer radical addition (ATRA) of a variety of haloalkanes onto olefins, one of the fundamental carbon-carbon bond-forming transformations i

SYNTHESIS OF ESTERS OF 2-SUBSTITUTED 4-KETOPENTANOIC ACIDS BY THE ALKYLATION OF CH-ACIDS USING CHLOROACETONE UNDER PHASE TRANSFER CATALYSIS CONDITIONS

Sizov, A. Yu.,Yanovskaya, L. A.,Dombrovskii, V. A.

, p. 410 - 411 (1990)

An improved method was developed for the synthesis of ethyl esters of 2-substituted 4-ketopentanoic acids by the alkylation of CH2(X)CO2Et using chloroacetone in the liquid-solid KOH (K2CO3 or Na2CO3)-DMF-PhCH2(Et)3NCl system.

Copper-Catalyzed Cross-Nucleophile Coupling of β-Allenyl Silanes with Tertiary C-H Bonds: A Radical Approach to Branched 1,3-Dienes

Shan, Qi-Chao,Hu, Lu-Min,Qin, Wei,Hu, Xu-Hong

supporting information, p. 6041 - 6045 (2021/08/03)

Described herein is a distinctive approach to branched 1,3-dienes through oxidative coupling of two nucleophilic substrates, β-allenyl silanes, and hydrocarbons appending latent functionality by copper catalysis. Notably, C(sp3)-H dienylation proceeded in a regiospecific manner, even in the presence of competitive C-H bonds that are capable of occurring hydrogen atom transfer process, such as those located at benzylic and other tertiary sites, or adjacent to an oxygen atom. Control experiments support the intermediacy of functionalized alkyl radicals.

METHOD OF CONTROLLING PLANTS

-

Page/Page column 29, (2018/02/28)

The present invention provides a method of controlling plants comprising applying to the plants, or to the locus of the plants a composition comprising (A) a compound of formula (I) selected from the group consisting of: Formula(I), or an N-oxide or salt form thereof, and (B) one or more further herbicides.

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