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(R)-(-)-2-propen-1-yl-4,6-dimethoxybenzoic acid (1-methyl-hept-6-enyl)ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

183384-69-2

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183384-69-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183384-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,3,8 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 183384-69:
(8*1)+(7*8)+(6*3)+(5*3)+(4*8)+(3*4)+(2*6)+(1*9)=162
162 % 10 = 2
So 183384-69-2 is a valid CAS Registry Number.

183384-69-2Downstream Products

183384-69-2Relevant academic research and scientific papers

Macrocycles by ring-closing-metathesis, XI: Syntheses of (R)-(+)- lasiodiplodin, zeranol and truncated salicylihalamides

Fuerstner, Alois,Seidel, Guenter,Kindler, Nicole

, p. 8215 - 8230 (2007/10/03)

Concise, flexible and high yielding approaches to the orsellinic acid type macrolides lasiodiplodin 1 and zeranol 3 are described which involve only metal-assisted or metal-catalyzed C-C-bond formations. Key steps are the efficient allylation of aryl triflates 14 and 25 either by Stille or by modified Suzuki coupling reactions, and the high yielding ring closure of the macrocyclic rings by RCM using the ruthenium carbene 18 as the catalyst. One of the synthesis intermediates, i.e. cycloalkene 16, can also be regarded as a truncated analogue of the potent anti-tumor agent salicylihalamide A 7. From the in-vitro cytotoxicity data of 16 it is possible to deduce first insights into the structure/activity relationship of salicylihalamide.

Macrocycle formation by ring-closing-metathesis. 2. An efficient synthesis of enantiomerically pure (R)-(+)-lasiodiplodin

Fuerstner, Alois,Kindler, Nicole

, p. 7005 - 7008 (2007/10/03)

A highly efficient and flexible route to the macrolide (R)-(+)-lasiodiplodin 1 and its de-O-methyl congener 2 is outlined, which is based on the formation of the 12-membered ring by ring-closing metathesis (RCM) as the key step.

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