958350-41-9 Usage
Uses
Used in Agricultural Research:
3”-O-tert-Butyl-2'-deoxyMugineic Acid tert-Butyl Diethyl Ester is used as a research compound for studying the mechanism of iron acquisition and utilization by graminaceous plants. Its protected structure allows for a better understanding of the role of phytosiderophores in iron uptake and transport in these plants, which can potentially lead to the development of more efficient crop varieties with improved iron uptake.
Used in Plant Physiology Studies:
In plant physiology research, 3”-O-tert-Butyl-2'-deoxyMugineic Acid tert-Butyl Diethyl Ester serves as a valuable tool for investigating the complex interactions between plants and essential nutrients, such as iron. Its protected form enables researchers to study the specific functions of Mugineic Acid and its derivatives in the context of plant growth and development, as well as their role in stress response and adaptation to different environmental conditions.
Used in Crop Improvement Programs:
3”-O-tert-Butyl-2'-deoxyMugineic Acid tert-Butyl Diethyl Ester can be employed in crop improvement programs aimed at enhancing the iron uptake and overall nutritional value of graminaceous plants. By understanding the mechanisms of iron acquisition and utilization in these plants, researchers can develop strategies to improve crop yields and nutritional quality, ultimately contributing to global food security and human health.
Check Digit Verification of cas no
The CAS Registry Mumber 958350-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,8,3,5 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 958350-41:
(8*9)+(7*5)+(6*8)+(5*3)+(4*5)+(3*0)+(2*4)+(1*1)=199
199 % 10 = 9
So 958350-41-9 is a valid CAS Registry Number.
958350-41-9Relevant academic research and scientific papers
EFFECTIVE PRODUCTION PROCESS FOR MUGINEIC ACID COMPOUND
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Page/Page column 10, (2009/10/01)
A method for producing mugineic acids, which is represented by the following scheme: (wherein R1 and R2 represent a hydrogen atom or a hydroxyl group, R3 represents a hydroxyl group or an amino group, R4 and R7 represent a hydrogen atom or a protecting group of a carboxyl group, R5 represents a protecting group of an amino group, R6 represents a protecting group of a carboxyl group, and R8 represents -OR9 (wherein R9 represents a protecting group of a hydroxyl group) or -NHR10 (wherein R10 represents a protecting group of an amino group)).
A practical synthesis of the phytosiderophore 2′-deoxymugineic acid: A key to the mechanistic study of iron acquisition by graminaceous plants
Namba, Kosuke,Murata, Yoshiko,Horikawa, Manabu,Iwashita, Takashi,Kusumoto, Shoichi
, p. 7060 - 7063 (2008/09/18)
(Chemical Equation Presented) Ironing out plant uptake: The phytosiderophores mugineic acid (MA) and deoxymugineic acid (DMA) were synthesized in a few steps with minimum use of protecting groups and workup/purification procedures (see scheme; Boc: tert-butoxycarbonyl) and their potencies in transporter-mediated iron(III) acquisition were tested. The sufficient supply of these compounds will enable study of the molecular mechanism of iron acquisition and utilization by graminaceous plants.
