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Carbamic acid, [[(1,1-dimethylethoxy)carbonyl]oxy](3-phenyl-2-propenyl)-, 1,1-dimethylethyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

159879-43-3

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159879-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159879-43-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,8,7 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 159879-43:
(8*1)+(7*5)+(6*9)+(5*8)+(4*7)+(3*9)+(2*4)+(1*3)=203
203 % 10 = 3
So 159879-43-3 is a valid CAS Registry Number.

159879-43-3Downstream Products

159879-43-3Relevant academic research and scientific papers

Palladium (0) catalyzed amination with N,O-bis-ter-Boc hydroxylamine. Synthesis of (+)-N6-hydroxylysine

Genet, Jean-Pierre,Thorimbert, Serge,Touzin, Anne-Marie

, p. 1159 - 1162 (1993)

Palladium-catalyzed reaction of allyl esters with (N,O)-bis-ter-Boc hydroxylamine 2 gives protected N-allylhydroxylamines. A synthetic application to (+)-N6-hydroxylysine component of mycobactin T is also described.

Studies in 3-oxy-assisted 3-aza Cope rearrangements

Gomes, Mario J. S.,Sharma, Lalit,Prabhakar, Sundaresan,Lobo, Ana M.,Gloria, Paulo M. C.

, p. 746 - 747 (2007/10/03)

On thermolysis appropriately substituted N-silyloxy-N-allyl enamines undergo smooth 3,3-sigmatropic rearrangments to the corresponding N-silyloxy imino ethers.

The Use of N,O-bis(tert-Butoxycarbonyl)-hydroxylamine in the Synthesis of N-Hydroxylamines and Hydroxamic Acids

Staszak, Michael A.,Doecke, Christopher W.

, p. 6021 - 6024 (2007/10/02)

N,O-bis(tert-butoxycarbonyl)-hydroxylamine has been used in the synthesis of 5-lipoxygenase inhibitor LY280810.In addition, this reagent utilized to synthesize a number of other hydroxylamine and hydroxamic acid derivatives in high yields.

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