934246-98-7 Usage
Description
(2E,4E,6R,7R)-ethyl7-(4-(dimethylamino) phenyl)-7-hydroxy-4,6-dimethylhepta-2,4-dienoate is a complex organic compound that features an ethyl ester group, a dimethylamino group attached to a phenyl ring, and a hydroxy group at the 7th position. It is a derivative of hepta-2,4-dienoic acid with multiple double bonds in the alkene chain, which may contribute to its potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
(2E,4E,6R,7R)-ethyl7-(4-(dimethylamino) phenyl)-7-hydroxy-4,6-dimethylhepta-2,4-dienoate is used as a bioactive molecule for the development of pharmaceuticals due to its unique structural features and potential medicinal properties.
Used in Agrochemical Industry:
In the agrochemical industry, (2E,4E,6R,7R)-ethyl7-(4-(dimethylamino) phenyl)-7-hydroxy-4,6-dimethylhepta-2,4-dienoate is used as a precursor or active ingredient in the synthesis of agrochemicals, leveraging its specific functional groups for targeted biological activity.
Used in Other Industries:
(2E,4E,6R,7R)-ethyl7-(4-(dimethylamino) phenyl)-7-hydroxy-4,6-dimethylhepta-2,4-dienoate may also be utilized in other industries that require complex organic compounds with specific structural features, such as in the development of advanced materials or as intermediates in chemical synthesis processes. Further research and analysis would be necessary to fully understand its properties, uses, and potential effects in these applications.
Check Digit Verification of cas no
The CAS Registry Mumber 934246-98-7 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 934246-98:
(8*9)+(7*3)+(6*4)+(5*2)+(4*4)+(3*6)+(2*9)+(1*8)=187
187 % 10 = 7
So 934246-98-7 is a valid CAS Registry Number.
934246-98-7Relevant articles and documents
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.
