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1-cyclopentylprop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25183-76-0

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25183-76-0 Usage

Physical State

Colorless liquid.

Odor

Sharp, sweet, and floral.

Common Uses

Flavor and fragrance ingredient in perfumes and cosmetics; intermediate in the synthesis of other organic compounds.

Health Hazards

Skin and eye irritant; toxic if ingested or inhaled in large amounts.

Check Digit Verification of cas no

The CAS Registry Mumber 25183-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,8 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25183-76:
(7*2)+(6*5)+(5*1)+(4*8)+(3*3)+(2*7)+(1*6)=110
110 % 10 = 0
So 25183-76-0 is a valid CAS Registry Number.

25183-76-0Upstream product

25183-76-0Relevant academic research and scientific papers

Dissociated nonsteroidal glucocorticoid receptor modulators; discovery of the agonist trigger in a tetrahydronaphthalene-benzoxazine series

Barker, Mike,Clackers, Margaret,Copley, Royston,Demaine, Derek A.,Humphreys, Davina,Inglis, Graham G. A.,Johnston, Michael J.,Jones, Haydn T.,Haase, Michael V.,House, David,Loiseau, Richard,Nisbet, Lesley,Pacquet, Francois,Skone, Philip A.,Shanahan, Stephen E.,Tape, Dan,Vinader, Victoria M.,Washington, Melanie,Uings, Iain,Upton, Richard,McLay, Iain M.,Macdonald, Simon J. F.

, p. 4216 - 4231 (2007/10/03)

The tetrahydronaphthalene-benzoxazine glucocorticoid receptor (GR) partial agonist 4b was optimized to produce potent full agonists of GR. Aromatic ring substitution of the tetrahydronaphthalene leads to weak GR antagonists. Discovery of an "agonist trigger" substituent on the saturated ring of the tetrahydronaphthalene leads to increased potency and efficacious GR agonism. These compounds are efficacy selective in an NFkB GR agonist assay (representing transrepression effects) over an MMTV GR agonist assay (representing transactivation effects). 52 and 60 have NFkB pIC50 = 8.92 (105%) and 8.69 (92%) and MMTV pEC50 = 8.20 (47%) and 7.75 (39%), respectively. The impact of the trigger substituent on agonism is modeled within GR and discussed. 36, 52, and 60 have anti-inflammatory activity in a mouse model of inflammation after topical dosing with 52 and 60, having an effect similar to that of dexamethasone. The original lead was discovered by a manual agreement docking method, and automation of this method is also described.

SUBSTITUTED OXAZINES AS GLUCOCORTICOID RECEPTOR MODULATORS

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Page/Page column 33, (2010/02/15)

The present invention is directed to compounds of formula (I), wherein R1 represents a C3-6cycloalkyl group; or a physiologically functional derivative thereof, pharmaceutical compositions comprising the compounds, the use of the compounds for the manufacture of medicaments particularly for the treatment of inflammatory and/or allergic conditions, processes for the preparation of the compounds, and chemical intermediates in the processes for the manufacture of the compounds.

Aluminum chloride (AlCl3) promotes selective oxidative deprotection of benzylic trimethylsilyl and tert-butyldimethylsilyl ethers to the corresponding carbonyl compounds with manganese dioxide (MnO2)

Firouzabadi, Habib,Etemadi, Shahrad,Karimi, Babak,Jarrahpour, Ali Asghar

, p. 4333 - 4339 (2007/10/03)

Various types of trimethylsilyl and tert-butyldimethylsilyl ethers of primary and secondary benzylic alcohols could be selectively converted to their corresponding carbonyl compounds with MnO2 in the presence of AlCl3 in good to excellent yields.

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