934246-96-5 Usage
Uses
Used in Pharmaceutical Synthesis:
(2E,4E,6R,7R)-ethyl7-hydroxy-4,6-dimethyl-7-(4-nitrophenyl)hepta-2,4-dienoate is used as a building block for the synthesis of pharmaceuticals. Its specific chemical structure allows it to be incorporated into the development of new drugs and medications, potentially leading to advancements in healthcare and medicine.
Used in Organic Chemistry Research:
(2E,4E,6R,7R)-ethyl7-hydroxy-4,6-dimethyl-7-(4-nitrophenyl)hepta-2,4-dienoate is used as a research compound in organic chemistry. Its unique properties and reactivity make it a valuable tool for studying various chemical reactions and mechanisms, contributing to the understanding of organic chemistry and the development of new synthetic methods.
Used in Chemical Industry:
(2E,4E,6R,7R)-ethyl7-hydroxy-4,6-dimethyl-7-(4-nitrophenyl)hepta-2,4-dienoate is used as an intermediate in the chemical industry. Its versatile chemical structure allows it to be used in the production of various organic compounds and materials, contributing to the development of new products and technologies in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 934246-96-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,4,2,4 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 934246-96:
(8*9)+(7*3)+(6*4)+(5*2)+(4*4)+(3*6)+(2*9)+(1*6)=185
185 % 10 = 5
So 934246-96-5 is a valid CAS Registry Number.
934246-96-5Relevant academic research and scientific papers
Efficient, enantioselective organocatalytic synthesis of trichostatin A
Zhang, Shilei,Duan, Wenhu,Wang, Wei
, p. 1228 - 1234 (2007/10/03)
An efficient, highly stereocontrolled total synthesis of trichostatin A (1) has been achieved in 9 steps with 17.4% overall yield and >99% optical purity from readily available achiral starting materials. The key features of this synthesis include the L-proline-promoted, highly enantioselective cross-aldol reaction as a crucial step for the construction of the C-6 chiral center and the minimization of racemization by final step oxidation of the OH group to a ketone at position 7.
