94136-77-3 Usage
Chemical structure
The compound has a propanetricarboxamide backbone with three attached groups, each containing an acetyl and phenylmethoxy moiety.
Applications
It is used in various industries, including pharmaceuticals, polymers, and other industries.
Building block
The compound's unique properties and functional groups make it ideal for use as a building block for creating novel materials and compounds with specific chemical and physical properties.
Drug delivery systems
It has potential use in drug delivery systems due to its complex structure and functional groups.
Catalyst
It can be used as a catalyst in chemical reactions, making it a valuable and versatile compound in the field of chemistry and materials science.
Molecular weight
The molecular weight of the compound is approximately 592.71 g/mol.
Solubility
The compound is likely to be soluble in organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO), but its solubility in water is not specified.
Stability
The stability of the compound under various conditions, such as temperature, pH, and light exposure, is not specified in the provided material.
Safety
The safety profile of the compound, including its toxicity, irritancy, and potential hazards, is not specified in the provided material. It is important to follow proper safety protocols and guidelines when handling and using this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 94136-77-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,3 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 94136-77:
(7*9)+(6*4)+(5*1)+(4*3)+(3*6)+(2*7)+(1*7)=143
143 % 10 = 3
So 94136-77-3 is a valid CAS Registry Number.
94136-77-3Relevant articles and documents
Artificial Siderophores. 1. Synthesis and Microbial Iron Transport Capabilities
Lee, Byung Hyun,Miller, Marvin J.,Prody, Catherine A.,Neilands, John B.
, p. 317 - 323 (2007/10/02)
Several di- and trihydroxamate analogues of natural microbial iron chelators have been prepared.The syntheses involved linkage of core structural units, including pyridinedicarboxylic acid, benzenetricarboxylic acid, nitrilotriacetic acid, and tricarballylic acid, by amide bonds to 1-amino-ω-(hydroxyamino)alkanes to provide the polyhydroxamates 1-5.The required protected (hydroxyamino)alkanes 8, 16, and 21 were prepared by different routes. 1-Amino-3-propane di-p-toluenesulfonate (8) was prepared from the N-protected aminopropanol 6 by oxidation to the aldehyde, formation of the substituted oxime, and reduction with NaBH3CN followed by deprotection of the Boc group.The pentyl derivatives 16 and 21 were made by direct alkylation with either benzyl acetohydroxamate or N-carbobenzoxy-O-benzylhydroxylamine.In Escherichia coli RW193 most of the analogues behaved nutritionally as ferrichrome.However, in E. coli AN193, a mutant lacking the ferrichrome receptor, capacity to use other natural siderophores was retained while response to all analogues was lost.
