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{[(3R,4S,7S,10S,11R)-15-Benzyloxy-10-(benzyloxycarbonyl-methyl-amino)-3-ethyl-11-hydroxy-7-isopropyl-3-methyl-6,9-dioxo-2-oxa-5,8-diaza-bicyclo[10.3.1]hexadeca-1(16),12,14-triene-4-carbonyl]-amino}-acetic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

556104-48-4

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556104-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 556104-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,6,1,0 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 556104-48:
(8*5)+(7*5)+(6*6)+(5*1)+(4*0)+(3*4)+(2*4)+(1*8)=144
144 % 10 = 4
So 556104-48-4 is a valid CAS Registry Number.

556104-48-4Downstream Products

556104-48-4Relevant academic research and scientific papers

Enantioselective total synthesis of ustiloxin D

Tanaka, Hiroko,Sawayama, Andrew M.,Wandless, Thomas J.

, p. 6864 - 6865 (2003)

Ustiloxin D and phomopsin A are potent antimitotic agents that bind to tubulin and interfere with cellular microtubule function. A synthetic strategy has been developed to allow access to both of the natural products as well as a variety of variants of th

Total synthesis of ustiloxin D and considerations on the origin of selectivity of the asymmetric allylic alkylation

Sawayama, Andrew M.,Tanaka, Hiroko,Wandless, Thomas J.

, p. 8810 - 8820 (2007/10/03)

As part of investigations into cell cycle checkpoint inhibitors, an asymmetric synthesis of the antimitotic natural product, ustiloxin D, has been completed. A salen-Al-catalyzed aldol reaction was employed to construct a chiral oxazoline 9 (99% yield, 98

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