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65025-95-8

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  • (3AR,4S,5R,6AS)-()-(TERT-BUTYLDIMETHYLSILYLOXYMETHYL)HEXAHYDRO-5-(TETRAHYDRO-2H-PYRAN-2-YLOXY)-2H-CYCLOPENTA[B]FURAN-2-ONE

    Cas No: 65025-95-8

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  • High Quality 2H-Cyclopenta[b]furan-2-One,4-[[[(1,1-Dimethylethyl)Dimethylsilyl]Oxy] Methyl]Hexahydro-5-[(Tetrahydro-2H-Pyran-2-yl)Oxy]-,(3aR,4S,5R,6aS)- on stock

    Cas No: 65025-95-8

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  • (3aR,4S,5R,6aS)-4-[[[(1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]hexahydro-5-[(tetrahydro-2H-pyran-2-yl)oxy]-2H-cyclopenta[b]furan-2-one

    Cas No: 65025-95-8

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65025-95-8 Usage

Uses

Intermediate in the preparation of prostaglandin derivatives

Check Digit Verification of cas no

The CAS Registry Mumber 65025-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,2 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65025-95:
(7*6)+(6*5)+(5*0)+(4*2)+(3*5)+(2*9)+(1*5)=118
118 % 10 = 8
So 65025-95-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H34O5Si/c1-19(2,3)25(4,5)22-12-14-13-10-17(20)23-15(13)11-16(14)24-18-8-6-7-9-21-18/h13-16,18H,6-12H2,1-5H3/t13-,14-,15+,16-,18?/m1/s1

65025-95-8SDS

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 (3aR,4S,5R,6aS)-4-[[tert-butyl(dimethyl)silyl]oxymethyl]-5-(oxan-2-yloxy)-3,3a,4,5,6,6a-hexahydrocyclopenta[b]furan-2-one

1.2 Other means of identification

Product number -
Other names Corey lactone

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65025-95-8 SDS

65025-95-8Downstream Products

65025-95-8Relevant articles and documents

The preparation method of the ruby's forefront

-

, (2018/04/01)

The invention relates to a preparation method of lubiprostone, and concretely relates to a preparation method of highly pure lubiprostone represented by formula (I). The method comprises the steps of reducing an initial compound, oxidizing, and hydrolyzing in order to obtain a target compound. Compared with other methods, the method provided by the invention has the advantages of good process reappearance, simple operation, high yield, low cost, high purity of the above obtained product, suitableness for industrialized production, and very high economic benefit.

Discovery of novel seven-membered prostacyclin analogues as potent and selective prostaglandin FP and EP3 Dual Agonists

Sugimoto, Isamu,Kambe, Tohru,Okino, Tomotaka,Obitsu, Tetsuo,Ohta, Nobukazu,Nishiyama, Taihei,Kinoshita, Akihiro,Fujimoto, Taku,Egashira, Hiromu,Yamane, Shinsaku,Shuto, Satoshi,Tani, Kousuke,Maruyama, Toru

supporting information, p. 107 - 112 (2017/12/12)

A novel series of prostaglandin analogues with a seven-membered ring scaffold was designed, synthesized, and evaluated for the functional activation of prostaglandin receptors to identify potent and subtype-selective FP and EP3 dual agonists. Starting fro

Corey lactone as key precursor for a facile synthesis of novel 1,2,3-triazole carbocyclic nucleosides via Click Chemistry

González-González, Carlos A.,Fuentes-Benítez, Aydeé,Cuevas-Yá?ez, Erick,Corona-Becerril, David,González-Romero, Carlos,González-Calderón, Davir

, p. 2726 - 2728 (2013/06/26)

Corey lactone (2) and Click Chemistry allowed for an efficient and facile approach to the synthesis of novel 1,2,3-triazole carbocyclic nucleosides (11 and 17) in good overall yields.

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