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methyl 1-(2-methoxy-6-methylphenyl)cyclopropanecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1185886-64-9

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1185886-64-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1185886-64-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,5,8,8 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1185886-64:
(9*1)+(8*1)+(7*8)+(6*5)+(5*8)+(4*8)+(3*6)+(2*6)+(1*4)=209
209 % 10 = 9
So 1185886-64-9 is a valid CAS Registry Number.

1185886-64-9Relevant academic research and scientific papers

Synthesis of Substituted Cyclopropanecarboxylates via Room Temperature Palladium-Catalyzed α-Arylation of Reformatsky Reagents

Greszler, Stephen N.,Halvorsen, Geoff T.,Voight, Eric A.

, p. 2490 - 2493 (2017)

The room temperature palladium-catalyzed cross-coupling of aromatic and heteroaromatic halides with Reformatsky reagents derived from 1-bromocyclopropanecarboxylates provides an exceptionally mild method for enolate α-arylation. The method is tolerant of a wide range of functionalities and dramatically shortens many of the existing routes to access widely used 1,1-disubstituted cyclopropanecarboxylate derivatives.

Modulators of the Cystic Fibrosis Transmembrane Conductance Regulator Protein and Methods of Use

-

Paragraph 2011, (2019/03/30)

The invention discloses compounds of Formula (I), wherein A1, R1, R2, R3, R4, and n are as defined herein. The present invention relates to compounds and their use in the treatment of cystic fibrosis, methods for their production, pharmaceutical compositions comprising the same, and methods of treating cystic fibrosis by administering a compound of the invention.

Remote electronic control in the regioselective reduction of succinimides: A practical, scalable synthesis of EP4 antagonist MF-310

Molinaro, Carmela,Gauvreau, Danny,Hughes, Gregory,Lau, Stephen,Lauzon, Sophie,Angelaud, Remy,O'Shea, Paul D.,Janey, Jacob,Palucki, Michael,Hoerrner, Scott R.,Raab, Conrad E.,Sidler, Rick R.,Belley, Michel,Han, Yongxin

supporting information; experimental part, p. 6863 - 6866 (2009/12/30)

(Chemical Equation Presented) A practical large-scale chromatography-free synthesis of EP4 antagonist MF-310, a potential new treatment for chronic inflammation, is presented. The synthetic route provided MF-310 as its sodium salt in 10 steps and 17% overall yield from commercially available pyridine dicarboxylate 7. The key features of this sequence include a unique regioselective reduction of succinimide 2 controlled by the electronic properties of a remote pyridine ring, preparation of cyclopropane carboxylic acid 3 via a Corey - Chaykovsky cyclopropanation, and a short synthesis of sulfonamide 5. 2009 American Chemical Society.

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