556038-76-7 Usage
Chiral molecule
Yes
Dioxolane ring
A five-membered ring containing two oxygen atoms
Nitro group
A functional group with the structure -NO2
Phenyl group
A six-membered aromatic ring with the formula C6H5
Methyl groups
Two -CH3 groups attached to the dioxolane ring
Stereochemistry
(4R,5S) configuration
4R
The 4th carbon atom in the dioxolane ring has the R configuration
5S
The 5th carbon atom in the dioxolane ring has the S configuration
Applications
Intermediate in the synthesis of pharmaceuticals and agrochemicals
Potential anti-inflammatory and analgesic agent
Importance of stereochemistry
The stereochemistry of the molecule is crucial for its biological activity
Research focus
Synthesis and characterization in organic chemistry
Check Digit Verification of cas no
The CAS Registry Mumber 556038-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,6,0,3 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 556038-76:
(8*5)+(7*5)+(6*6)+(5*0)+(4*3)+(3*8)+(2*7)+(1*6)=167
167 % 10 = 7
So 556038-76-7 is a valid CAS Registry Number.
556038-76-7Relevant academic research and scientific papers
Total synthesis of the duocarmycins
Yamada, Ken,Kurokawa, Toshiki,Tokuyama, Hidetoshi,Fukuyama, Tohru
, p. 6630 - 6631 (2007/10/03)
The total synthesis of (+)-duocarmycin A and SA through a common indoline intermediate is described. The key reactions include selective lithiation of a 2,6-dibromoiodobenzene derivative and diastereoselective addition to a chiral nitroalkene, copper-mediated aryl amination, and addition of aryllithium to azlactones. Copyright
