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(2S)-N4-benzyloxycarbonyl-N1,N2-di-tert-butoxycarbonyl-1,2,4-triaminobutane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

156604-31-8

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156604-31-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156604-31-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,6,0 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 156604-31:
(8*1)+(7*5)+(6*6)+(5*6)+(4*0)+(3*4)+(2*3)+(1*1)=128
128 % 10 = 8
So 156604-31-8 is a valid CAS Registry Number.

156604-31-8Downstream Products

156604-31-8Relevant academic research and scientific papers

BACTERIAL EFFLUX PUMP INHIBITORS

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Page/Page column 40, (2017/09/09)

Disclosed herein are compounds of formula I: and salts thereof. Also disclosed are compositions comprising compounds of formula I and methods using compounds of formula I.

New analogues of agmatine with higher affinity to imidazoline receptors

Treder, Adam P.,Andruszkiewicz, Ryszard,Zgoda, W?odzimierz,Ford, Celeste,Hudson, Alan L.

scheme or table, p. 1009 - 1011 (2009/09/25)

Compilation of agmatine structure and imidazoline ring leads to a new family of imidazoline/α2-adrenoceptor ligands, 4(5)-(2-aminoethyl)imidazoline derivatives. Constraining of the guanidine moiety into heterocyclic ring improved the affinities of the resultant fusion compounds in comparison to agmatine itself. In this work, the synthetic approach and results for I1, I2, and α2-adrenoceptors affinities are reported.

A new approach to the synthesis of selectively protected (2S)-1,2,4-triaminobutane derivatives

Treder, Adam P.,Walkowiak, Aleksandra,Zgoda, Wlodzimierz,Andruszkiewicz, Ryszard

, p. 2281 - 2283 (2007/10/03)

An efficient synthesis of selectively protected (2S)-1,2,4-triaminobutane from L-glutamic acid via (2S)-N4-benzyloxycarbonyl-2,4- diaminobutanamid is described. Georg Thieme Verlag Stuttgart.

Selectively Protected Chiral 1,2,4-Triaminobutanes and Chiral Vicinal 1,2-Diamines

Altman, Janina,Ben-Ishai, Dov,Beck, Wolfgang

, p. 887 - 894 (2007/10/02)

Stepwise t-butoxycarbonylation of (S)-5-aminomethyl-2-pyrrolidone to mono-, di- and triacylated compounds has been elaborated.Ring opening of (S)-5-(Boc-aminomethyl)-N1-Boc-2-pyrrolidone with LiOH afforded the Boc-protected 4,5-diaminovaleric a

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