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(Z)-ethyl 2-benzyloxy-4,5-dimethoxy-α-nitrocinnamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1034028-87-9

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1034028-87-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1034028-87-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,4,0,2 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1034028-87:
(9*1)+(8*0)+(7*3)+(6*4)+(5*0)+(4*2)+(3*8)+(2*8)+(1*7)=109
109 % 10 = 9
So 1034028-87-9 is a valid CAS Registry Number.

1034028-87-9Relevant academic research and scientific papers

Synthesis of lamellarin U and lamellarin G trimethyl ether by alkylation of a deprotonated α-aminonitrile

Liermann, Johannes C.,Opatz, Till

, p. 4526 - 4531 (2008/09/21)

(Chemical Equation Presented) 1,2,3,4-Tetrahydroisoquinoline-1- carbonitriles can serve as starting materials for the one-pot synthesis of 5,6-dihydropyrrolo[2,1a]isoquinolines and 1-benzyl-3,4-dihydroisoquinolines. The latter compounds were transformed to lamellarin G trimethyl ether and lamellarin U in short reaction sequences. This method allows the introduction of acid-sensitive protecting groups for the phenolic hydroxy functions which would be cleaved under the harsh conditions of the classical Bischler-Napieralski reaction.

Total synthesis of natural and unnatural lamellarins with saturated and unsaturated D-rings

Ploypradith, Poonsakdi,Petchmanee, Thaninee,Sahakitpichan, Poolsak,Litvinas, Nichole D.,Ruchirawat, Somsak

, p. 9440 - 9448 (2007/10/03)

(Chemical Equation Presented) Twenty-eight natural and unnatural lamellarins with either a saturated or an unsaturated D-ring were synthesized according to our developed synthetic route. The key step involved the Michael addition/ring closure (Mi-RC) of the benzyldihydroisoquinoline and α-nitrocinnamate derivatives, which provided the 2-carboethoxypyrrole intermediates in moderate to good yields (up to 78% yield). Subsequent hydrogenolysis/lactonization furnished lamellarins with a saturated D-ring in excellent yields (up to 93% yield). DDQ oxidation of the saturated lamellarin acetates led directly to the corresponding unsaturated analogues in 54-95% yield. In addition, only two steps in our developed strategy require column chromatography.

Utility of polymer-supported reagents in the total synthesis of lamellarins

Ploypradith, Poonsakdi,Kagan, Rachel Kirk,Ruchirawat, Somsak

, p. 5119 - 5125 (2007/10/03)

Four solid-supported reagents have been utilized in the multistep synthesis of lamellarins. The use of Amberlyst A-26 Br3- and polymer bound pyridine hydrobromide perbromide (PVPHP) for keto α-bromination of the less studied ortho-su

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