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benzotriazol-1-yl-dibenzylamino-acetic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

230302-45-1

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230302-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 230302-45-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,0,3,0 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 230302-45:
(8*2)+(7*3)+(6*0)+(5*3)+(4*0)+(3*2)+(2*4)+(1*5)=71
71 % 10 = 1
So 230302-45-1 is a valid CAS Registry Number.

230302-45-1Downstream Products

230302-45-1Relevant academic research and scientific papers

Synthesis of the four diastereoisomers of the N-terminal amino acids of nikkomycins via aminoalkylation with preformed ternary iminium salts

Delbos-Krampe, Jeanne,Risch, Nikolaus,Fl?rke, Ulrich

, p. 414 - 423 (2004)

An efficient and convenient two step synthesis of each of the four possible diastereoisomers of the N-terminal amino acid component of nikkomycins is described. We first synthesized α-amino-β-oxo acids by aminoalkylation of ketones with iminium salts. The second step using Pearlman's catalyst gave directly nonnatural and natural precursors 13-16 of nikkomycins 1 which were easily separated by chromatography on silica gel.

ALDOSTERONE SYNTHASE AND/OR 11β-HYDROXYLASE INHIBITORS

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Page/Page column 50-51, (2008/06/13)

The present invention provides a compound of formula (I). Said compound is inhibitor of CYP11B2 and/or CYP11B1, and thus can be employed for the treatment of a disorder or disease mediated by CYP11B2 and/or CYP11B1.

Efficient synthesis of racemic α-aryl-α-amino acid esters via aminoalkylation with in situ generated glycine cation equivalents

Grumbach, Hans-Joachim,Merla, Beatrix,Risch, Nikolaus

, p. 1027 - 1033 (2007/10/03)

Iminium salts generated in situ from ethyl glyoxylate, secondary amines and 1-H-benzotriazole are demonstrated to be excellent reagents for the regioselective mono-aminoalkylation of indoles, phenols, furans and pyrroles. This method provides a simple and

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