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Ethyl 1-[2-(benzyloxy)-2-oxoethyl]-2-oxocyclohexanecarboxylate is a complex organic compound with the molecular formula C19H22O5. It is a derivative of cyclohexane, featuring a cyclohexane ring with a carboxylate group at the 1-position and a 2-oxoethyl group at the 2-position. The 2-oxoethyl group is further modified with a benzyloxy group, which is a benzyl group attached to an oxygen atom. ethyl 1-[2-(benzyloxy)-2-oxoethyl]-2-oxocyclohexanecarboxylate is characterized by its ester and ketone functional groups, which contribute to its reactivity and potential applications in organic synthesis. It is often used as an intermediate in the synthesis of pharmaceuticals and other complex organic molecules due to its ability to undergo various chemical transformations.

6343-03-9

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6343-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6343-03-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6343-03:
(6*6)+(5*3)+(4*4)+(3*3)+(2*0)+(1*3)=79
79 % 10 = 9
So 6343-03-9 is a valid CAS Registry Number.

6343-03-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-oxo-1-(2-oxo-2-phenylmethoxyethyl)cyclohexane-1-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 1-[2-(benzyloxy)-2-oxoethyl]-2-oxocyclohexanecarboxylate

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:6343-03-9 SDS

6343-03-9Relevant academic research and scientific papers

Rearrangements of α-Diazo-β-hydroxyketones for the Synthesis of Bicyclo[m.n.1]alkanones

Li, Zhengning,Lam, Shuk Mei,Ip, Ignatius,Wong, Wing-Tak,Chiu, Pauline

supporting information, p. 4464 - 4467 (2017/09/11)

Rhodium-catalyzed decomposition of fused bicyclic α-diazo-β-hydroxyketones results in good yields of bridged bicyclo[m.n.1]ketones via a rearrangement pathway.

Photoinduced electron transfer promoted radical ring expansion and cyclization reactions of α-(ω-carboxyalkyl) β-keto esters

Nishikawa, Keisuke,Ando, Tomoki,Maeda, Kousuke,Morita, Toshio,Yoshimi, Yasuharu

supporting information, p. 636 - 638 (2013/04/10)

Photoinduced electron transfer (PET) promoted decarboxylation of α-(ω-carboxyalkyl) β-keto esters undergoes radical ring expansion and cyclization reactions. This mild and environmentally friendly method can provide one-carbon expanded γ-keto esters and b

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