4607-41-4 Usage
Uses
Used in Pharmaceutical Industry:
Benzenepropanoic acid, 3-hydroxy-α-oxo-, is used as a reactant for the preparation of (±)-thaxtomin A, a compound with diverse biological activities. These activities include phytotoxic, fungicidal, and antiviral properties, making it a valuable compound for the development of new drugs and treatments in the pharmaceutical industry.
Used in Agricultural Industry:
In the agricultural industry, Benzenepropanoic acid, 3-hydroxy-α-oxo-, plays a role in the synthesis of compounds with fungicidal and phytotoxic properties. These compounds can be used to protect crops from fungal infections and other plant diseases, thereby increasing crop yield and quality.
Used in Chemical Research:
Due to its unique chemical structure, Benzenepropanoic acid, 3-hydroxy-α-oxo-, is also utilized in chemical research for the development of new synthetic methods and the study of reaction mechanisms. This contributes to the advancement of chemical science and the discovery of new compounds with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 4607-41-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,0 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4607-41:
(6*4)+(5*6)+(4*0)+(3*7)+(2*4)+(1*1)=84
84 % 10 = 4
So 4607-41-4 is a valid CAS Registry Number.
4607-41-4Relevant articles and documents
A one-pot multicomponent coupling/cyclization for natural product herbicide (±)-thaxtomin A
Bourgault, Jean Paul,Maddirala, Amarendar Reddy,Andreana, Peter R.
supporting information, p. 8125 - 8127 (2015/01/08)
Herbicide (±)-thaxtomin A has been synthesized in a one-pot process with a 32% isolated yield. A multicomponent coupling reaction was utilized to prepare in situ a dipeptide precursor which then sequentially underwent an alkaline mediated keto-amide cyclization to provide the target molecule. Adjustment of diastereoselectivity was achieved using microwave-induced irradiation. The approach incorporates atom economy and reaction efficiency and allows for facile library development. This journal is
Application of ruthenium-induced macrocyclization for the construction of macrocyclic depsipeptides
Venkatraman, Srikanth,Njoroge, F. George,Girijavallabhan, Viyyoor,McPhail, Andrew T.
, p. 3152 - 3155 (2007/10/03)
The synthesis of a biaryl ether containing macrocyclic depsipeptide 1 was achieved in 6% overall yield. The desired macrocycle was constructed by cyclization of a phenol into η6-ruthenium complex. The ruthenium metal was subsequently photolytically deprotected to obtain the macrocycle.
