194303-33-8 Usage
Description
2-Pentenoic acid, 5-[2-(acetyloxy)-3,4,6-trimethyl-5-(phenylmethoxy)phenyl]-3-methyl-, methyl ester, (2E)is a complex organic chemical compound characterized by a pentenoic acid group and a methyl ester group. It features a long aromatic side chain with multiple methyl and phenyl groups, and an acetyloxy group adds further complexity to its structure. 2-Pentenoic acid,
5-[2-(acetyloxy)-3,4,6-trimethyl-5-(phenylmethoxy)phenyl]-3-methyl-,
methyl ester, (2E)is in the (2E)configuration, which refers to the specific arrangement of the double bond.
Uses
Used in Pharmaceutical Industry:
2-Pentenoic acid, 5-[2-(acetyloxy)-3,4,6-trimethyl-5-(phenylmethoxy)phenyl]-3-methyl-, methyl ester, (2E)is used as an intermediate in the synthesis of pharmaceutical compounds due to its unique structure and functional groups. Its potential applications may include the development of new drugs or the modification of existing ones to improve their efficacy and safety.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2-Pentenoic acid, 5-[2-(acetyloxy)-3,4,6-trimethyl-5-(phenylmethoxy)phenyl]-3-methyl-, methyl ester, (2E)can be utilized as a building block for the creation of various complex organic molecules. Its versatility and the presence of multiple functional groups make it a valuable component in the synthesis of specialty chemicals, agrochemicals, or other advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 194303-33-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,3,0 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 194303-33:
(8*1)+(7*9)+(6*4)+(5*3)+(4*0)+(3*3)+(2*3)+(1*3)=128
128 % 10 = 8
So 194303-33-8 is a valid CAS Registry Number.
194303-33-8Relevant articles and documents
Chiral palladium complex-catalyzed synthesis of optically active vinylchroman
Mizuguchi,Achiwa
, p. 1209 - 1211 (1997)
Optically active vinylchroman (1) was synthesized from a corresponding allyl carbonate (2) by catalytic and asymmetric allylic substitution with palladium complexes of chiral bisphosphine ligands. The reactivity and selectivity of the various chiral bisph
