329362-94-9 Usage
Functional Groups
Phenyl group: A benzene ring attached to the 7th carbon atom.
Methoxy group: Attached to the 5th carbon atom.
Hydroxyl group: Present at the 1st carbon atom.
Stereochemistry
Configuration: (2E,4S,5S,6E)
Indicates the positioning of the double bonds (E configuration) and the stereochemistry at specific carbon atoms (S configuration).
Potential Applications
Pharmaceuticals: Due to its complex structure, it might exhibit biological activity that could be useful in drug development.
Chemical Synthesis: Can serve as a starting material or intermediate in organic synthesis.
Biochemistry: May be of interest for studying enzyme reactions or biological processes due to its structural complexity.
Further Research Needed
To fully understand its properties, potential uses, and any biological activity it may possess.
Check Digit Verification of cas no
The CAS Registry Mumber 329362-94-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,3,6 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 329362-94:
(8*3)+(7*2)+(6*9)+(5*3)+(4*6)+(3*2)+(2*9)+(1*4)=159
159 % 10 = 9
So 329362-94-9 is a valid CAS Registry Number.
329362-94-9Relevant academic research and scientific papers
Total synthesis of (+)-crocacin C
Chakraborty, Tushar K,Jayaprakash, Sarva,Laxman, Pasunoori
, p. 9461 - 9467 (2007/10/03)
The total synthesis of potent antifungal and cytotoxic agent (+)-crocacin C in optically pure form following a convergent strategy is described here in detail. The synthesis also established the absolute stereochemistry of the molecule having a (6S,7S,8R,9S) configuration. While C8 and C9 stereocenters were built following a Ti(IV)-mediated diastereoselective 'non-Evans' aldol reaction based on 2-oxazolidinethione chiral auxiliary, lithium dimethylcuprate opening of a C6-C7 chiral epoxide prepared by Sharpless epoxidation method established the remaining two stereocentres.
Total synthesis of (+)-crocacin C
Chakraborty, Tushar K.,Jayaprakash, Sarva
, p. 497 - 499 (2007/10/03)
The first synthesis of (+)-crocacin C (3) in optically pure form is achieved following a convergent strategy. The synthesis also establishes the absolute stereochemistries of this novel class of potent antifungal and highly cytotoxic compounds. The naturally occurring crocacin C has (6S,7S,8R,9S) configuration, which is also the same for other congeners of the family, crocacins A, B and D.
