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DIETHYL 4-OXOCYCLOHEXANE-1,1-DICARBOXYLATE is a chemical compound with the formula C14H20O5. It is categorized as an ester, as it is derived from carboxylic acid and alcohol. It's characterized by two carboxylate ester functional groups coming from Cyclohexanone-1,1-dicarboxylic acid, an organic compound with two carboxylic acid functional groups on the same carbon atom. It is used as an intermediate in organic synthesis, indicating its significant role in producing other chemicals. The properties of this chemical depend on its structure and, like other organic compounds, can participate in various chemical reactions.

55704-60-4

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55704-60-4 Usage

Uses

Used in Organic Synthesis:
DIETHYL 4-OXOCYCLOHEXANE-1,1-DICARBOXYLATE is used as an intermediate for [application reason] in the production of other chemicals. Its role is crucial in organic synthesis, allowing for the creation of a wide range of compounds with various applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 55704-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,0 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55704-60:
(7*5)+(6*5)+(5*7)+(4*0)+(3*4)+(2*6)+(1*0)=124
124 % 10 = 4
So 55704-60-4 is a valid CAS Registry Number.
InChI:InChI=1S/C12H18O5/c1-3-16-10(14)12(11(15)17-4-2)7-5-9(13)6-8-12/h3-8H2,1-2H3

55704-60-4SDS

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 Diethyl 4-oxocyclohexane-1,1-dicarboxylate

1.2 Other means of identification

Product number -
Other names diethyl 4-oxocyclohexane-1,1-dicarboxylate

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:55704-60-4 SDS

55704-60-4Relevant academic research and scientific papers

Identification of potent, selective and orally bioavailable phenyl ((R)-3-phenylpyrrolidin-3-yl)sulfone analogues as RORγt inverse agonists

Lu, Zhonghui,Duan, James J.-W.,Xiao, Haiyun,Neels,Wu, Dauh-Rurng,Weigelt, Carolyn A.,Sack, John S.,Khan,Ruzanov, Max,An, Yongmi,Yarde, Melissa,Karmakar, Ananta,Vishwakrishnan, Sureshbabu,Baratam, Venkata,Shankarappa, Harisha,Vanteru, Sridhar,Babu, Venkatesh,Basha, Mushkin,Kumar Gupta, Arun,Kumaravel, Selvakumar,Mathur, Arvind,Zhao, Qihong,Salter-Cid, Luisa M.,Carter, Percy H.,Murali Dhar

, p. 2265 - 2269 (2019/07/03)

An X-ray crystal structure of one of our previously discovered RORγt inverse agonists bound to the RORγt ligand binding domain revealed that the cyclohexane carboxylic acid group of compound 2 plays a significant role in RORγt binding, forming four hydrog

Oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad spectrum antibacterial agents

Singh, Sheo B.,Kaelin, David E.,Wu, Jin,Miesel, Lynn,Tan, Christopher M.,Meinke, Peter T.,Olsen, David,Lagrutta, Armando,Bradley, Prudence,Lu, Jun,Patel, Sangita,Rickert, Keith W.,Smith, Robert F.,Soisson, Stephen,Wei, Changqing,Fukuda, Hideyuki,Kishii, Ryuta,Takei, Masaya,Fukuda, Yasumichi

supporting information, p. 609 - 614 (2014/06/09)

Bacterial resistance is eroding the clinical utility of existing antibiotics necessitating the discovery of new agents. Bacterial type II topoisomerase is a clinically validated, highly effective, and proven drug target. This target is amenable to inhibit

BRIDGED BICYCLIC COMPOUNDS FOR THE TREATMENT OF BACTERIAL INFECTIONS

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Page/Page column 68, (2013/03/26)

Novel bridged bicyclic compounds are disclosed herein, along with their pharmaceutically acceptable salts, hydrates and prodrugs. Also disclosed are compositions comprising such compounds, methods of preparing such compounds and methods of using such compounds as antibacterial agents. The disclosed compounds, their pharmaceutically acceptable salts, hydrates and prodrugs, as well as compositions comprising such compounds, salts, hydrates and prodrugs, are useful for treating bacterial infections and associated diseases and conditions.

HIV INTEGRASE INHIBITORS

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Page/Page column 64-65, (2012/06/30)

The disclosure generally relates to the novel compounds of formula (I), including their salts, which inhibit HIV integrase and prevent viral integration into human DNA. This action makes the compounds useful for treating HIV infection and AIDS. The invent

Synthesis of cobalt-substituted 1,3-diene complexes with unusual structures and their exo-selective Diels-Alder reactions

Wright, Marcus W.,Smalley Jr., Terrence L.,Welker, Mark E.,Rheingold, Arnold L.

, p. 6777 - 6791 (2007/10/02)

The synthesis and characterization (including crystallographic data) of several substituted-pyridine (Rpyr) cobalt bis(dimethylglyoxime) 1,3-butadiene complexes (R = H, tBu, 3,5-diMe, and N,N-dimethylamino) and their Diels-Alder reactions with a variety of dienophiles are reported here. The cobalt-carbon bonds in the Diels-Alder cycloadducts can be cleaved so that cobalt complexes as well as functionalized organic cycloadducts are recovered. Through these cobalt-carbon bond cleavage reactions, cobalt-diene complexes can serve as synthons for a variety of 1,3-dienes such as 1,3-butadiene, 2-(trimethylsiloxy)- 1,3-butadiene, iodoprene, (E)-1-methoxy-3-(trimethylsiloxy)-1,3-butadiene (Danishefsky's diene), and 1,2-dichloro-1,3-butadiene. The preparation of several cobalt-substituted 1,2- and 1,3-pentadiene complexes and highly exo-selective Diels-Alder reactions of the 1,3-pentadiene complexes are then discussed followed by demetalation reactions of these more highly substituted cobalt cycloadducts. These demetalation reactions maintain the stereochemical integrity found in the metal cycloadducts and also lead to cobalt recovery.

FACILE SYNTHESIS OF 4-CARBETHOXYCYCLOHEXANONE

Sanchez, Ignacio H.,Ortega, Armando,Garcia, Gabriel,Larraza, Maria Isabel,Flores, Humberto J.

, p. 141 - 150 (2007/10/02)

A facile decarboalkoxylative route to 4-carbethoxycyclohexanone (1) from the tricarbethoxy derivative 3 is described.

LACTONE FORMATION USING TMSI

Walley, D.R.,Belletire, J.L.

, p. 401 - 406 (2007/10/02)

Iodotrimethylsilane facilitates the rapid lactonization of alcohol ester 2 under remarkably mild conditions.

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