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(E)-3-[2-cyclopropyl-4-(4-fluoro-phenyl)-quinolin-3-yl]-N-methoxy-N-methyl-acrylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

141750-56-3

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141750-56-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141750-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,7,5 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141750-56:
(8*1)+(7*4)+(6*1)+(5*7)+(4*5)+(3*0)+(2*5)+(1*6)=113
113 % 10 = 3
So 141750-56-3 is a valid CAS Registry Number.

141750-56-3Relevant academic research and scientific papers

Process for the manufacture of organic compounds

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Page 11, (2010/02/03)

The invention relates to a process for the manufacture of a compound of formula or a salt, especially a pharmaceutically acceptable salt with a base, thereof or a lactone thereof wherein the element represents —CH2—CH2— or —CH═CH— an

Stereoselective reduction of β,δ-diketo esters. A novel strategy for the synthesis of artificial HMG-CoA reductase inhibitors

Hiyama,Reddy,Minami,Hanamoto

, p. 350 - 363 (2007/10/02)

Condensation of N-methoxy-N-methyl amides with the dianions of acetoacetates gives in good yields β,δ-diketo esters, which are reduced with Et2BOMe-NaBH4 in tetrahydrofuran-methanol highly selectively to give syn-β,δ-dihydroxy esters in one step. Similarly, the β,δ-diketo esters of the Taber's chiral alcohol or its enantiomer respectively are reduced to give syn-β,δ-dihydroxy esters of moderate enantiomeric excess. Higher diastereo- and enantioselectivity were achieved by reduction of the β,δ-diketo esters of the Taber's chiral alcohol or its enantiomer successively with diisobutylalane and with Et2BOMe-NaBH4. The resulting syn-diol esters were hydrolyzed and lactonized to give various types of β-hydroxy-δ-lactones commonly found in artificial HMG-CoA reductase inhibitors.

Optically active esters of 7-substituted 3,5-difunctionalized 6-heptenoic acids

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, (2008/06/13)

The present invention provides optically active esters of 7-substituted 3,5-difunctionalized 6-heptenoic acids represented by the following formula: STR1 wherein R is a substituted or unsubstituted aromatic group, a substituted or unsubstituted heteroarom

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