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(3R,4R,5R)-3-hydroxy-5-((S)-hydroxy(phenyl)methyl)-1-methyl-4-phenylpyrrolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

608128-76-3

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608128-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 608128-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,8,1,2 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 608128-76:
(8*6)+(7*0)+(6*8)+(5*1)+(4*2)+(3*8)+(2*7)+(1*6)=153
153 % 10 = 3
So 608128-76-3 is a valid CAS Registry Number.

608128-76-3Downstream Products

608128-76-3Relevant academic research and scientific papers

Magnesium-coordinated chelation control in 1,3-dipolar cycloaddition of chiral α-alkoxymethyl ether nitrile oxide: Application to the synthesis of (-)/(-)- cis -clausenamide

Tanda, Kazuhiro,Toyao, Atsushi,Watanabe, Akiko,Sakamoto, Masanori,Yamasaki, Tetsuo

, (2014)

A facile regio- and diastereoselective nitrile oxide cycloaddition method using magnesium-coordinated chelation control of chiral α-alkoxymethyl ether nitrile oxide is reported. This reaction could be successfully applied as a key step in both the formal total synthesis of (-)-clausenamide and the total synthesis of (-)-cis-clausenamide.

Concise asymmetric synthesis of fully substituted isoxazoline-N-Oxide through lewis base catalyzed nitroalkene activation

Zhong, Cheng,Gautam, Lekh Nath S.,Petersen, Jeffrey L.,Akhmedov, Novruz G.,Shi, Xiaodong

supporting information; experimental part, p. 8605 - 8609 (2010/11/03)

(Figure Presented) Transforming isoxazoline-N-oxides: A concise asymmetric synthesis of isoxazoline-N-oxides is reported through secondary amine Lewis base catalyzed nitroalkene activation and sequential intermolecular condensation with aldehydes and ylides. Application of camphor-derived chiral sulfur ylides gave the enantiomeric-enriched isoxazolineN-oxides in excellent yields and stereoselectivity. Simple transformations of isoxazoline-N-oxide led to the gramscale synthesis of a (-)-clausenamide analogue in four steps, with excellent stereochemistry control (see scheme).

Synthesis and activity in enhancing long-term potentiation (LTP) of clausenamide stereoisomers

Feng, Zhiqiang,Li, Xingzhou,Zheng, Guojun,Huang, Liang

scheme or table, p. 2112 - 2115 (2009/12/03)

Clausenamide, isolated from aqueous extract of dry leaves of Clausena lansium, a Chinese folk medicine, was found to have potent activity in enhancing LTP and show nootropic activity in animal tests. In order to discovery more potent stereoisomers and to

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