152089-13-9 Usage
Structure
The compound consists of an azetidine ring, a carboxylic acid group, a phenyl group, a 1,1-dimethylethyl ester, and a dimethylsilyl group.
Azetidine Ring
A four-membered nitrogen-containing ring.
Carboxylic Acid Group
A functional group with the formula -COOH.
Phenyl Group
A six-membered aromatic ring with alternating single and double carbon-carbon bonds.
1,1-Dimethylethyl Ester
An ester derived from the reaction of the carboxylic acid group with 1,1-dimethylethyl alcohol (tert-butyl alcohol).
Dimethylsilyl Group
A functional group with the formula -Si(CH3)2.
Stereochemistry
(3R,4S)The stereochemistry of the compound indicates the relative positions of substituents on the molecule.
Potential Applications
Medicinal chemistry, materials science, or other fields due to its unique structure and properties.
Complexity
The compound has a complex structure with multiple functional groups and stereochemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 152089-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,0,8 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 152089-13:
(8*1)+(7*5)+(6*2)+(5*0)+(4*8)+(3*9)+(2*1)+(1*3)=119
119 % 10 = 9
So 152089-13-9 is a valid CAS Registry Number.
152089-13-9Relevant academic research and scientific papers
Ojima, Iwao,Sun, Chung Ming,Zucco, Martine,Park, Young Boon,Duclos, Olivier,Kuduk, Scott
, p. 4149 - 4152 (1993)
Taxotere, a highly promising anticancer drug, is synthesized through an efficient coupling of 7,10-diTroc-10-deacetylbaccatin III with enantiomerically pure (3R,4S)-1-tBOC-3-EEO- 4-phenylazetidin-2-one which is obtained via chiral ester enolate - imine cyclocondensation.
