93605-98-2 Usage
Carbon Atoms
15
Functional Groups
Hydroxy group attached to the 7th carbon
Methyl ester group attached to the 2nd carbon
Phenylmethoxy group attached to the 15th carbon
Double Bond Configuration
E, E, E
Applications
Organic Chemistry: Used in various organic synthesis reactions.
Pharmaceuticals: Potential applications in pharmaceutical development.
Agrochemicals: Potential applications in the development of agricultural chemicals.
Research Interest
Subject for further research and experimentation in chemical synthesis and analysis due to its unique structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 93605-98-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,0 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 93605-98:
(7*9)+(6*3)+(5*6)+(4*0)+(3*5)+(2*9)+(1*8)=152
152 % 10 = 2
So 93605-98-2 is a valid CAS Registry Number.
93605-98-2Relevant academic research and scientific papers
DIELS-ALDER CYCLIZATION OF 2,8,10-UNDECATRIENALS AS A ROUTE TO 1,2,3,4,4a,5,6,8a-OCTAHYDRONAPHTHALENES
Marshall, James A.,Audia, James E.,Grote, Jonathan,Shearer, Barry G.
, p. 2893 - 2902 (2007/10/02)
2,8,10-Undecatrienals have been found to undergo facile Diels-Alder cyclization upon treatment with alkylaluminum chlorides in methylene chloride at low temperature.The reaction is highly endo-selective.Protected alcohol substituents at the C-4 and C-7 po
Intramolecular Diels-Alder Cyclization of Conjugated Aldehydes. Synthesis of a Chlorothricolide Intermediate
Marshall, James A.,Audia, James E.,Grote, Jonathan
, p. 5277 - 5279 (2007/10/02)
Various substituted 2,8,10-undecatrienals have been found to undergo facile intramolecular Diels-Alder cyclization in the presence of dialkylaluminium chlorides to give bicyclooctahydronaphthalenecarboxaldehydes with high endo selectivity.The metho
