1455091-06-1 Usage
Molecular structure
Consists of a benzene ring with phenoxy and sulfonyl groups attached, a carboxylic acid group, an ester group, a methoxycarbonylmethyl group, and a toluene-4-sulfonylamino substituent.
Molecular weight
High, due to the complexity of its structure.
Potential applications
May be used in pharmaceutical or chemical research, as the compound has a unique and complex structure.
Functional groups
Carboxylic acid, ester, and methoxycarbonyl groups contribute to its chemical reactivity and properties.
Aromatic character
The presence of a benzene ring with phenoxy and sulfonyl groups imparts aromatic character to the compound.
Substituents
The presence of a methoxycarbonylmethyl group and a toluene-4-sulfonylamino substituent influences the compound's chemical properties and reactivity.
Further analysis
Additional research and analysis are required to fully understand the properties and potential applications of this complex compound.
Check Digit Verification of cas no
The CAS Registry Mumber 1455091-06-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,5,0,9 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1455091-06:
(9*1)+(8*4)+(7*5)+(6*5)+(5*0)+(4*9)+(3*1)+(2*0)+(1*6)=151
151 % 10 = 1
So 1455091-06-1 is a valid CAS Registry Number.
1455091-06-1Relevant articles and documents
Preparation method of isoquinoline derivative
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, (2021/02/10)
Disclosed is a preparation method of an isoquinoline derivative. A preparation method of a compound represented by a general formula II, i.e., 4-hydroxy-1-methyl-7-phenoxy isoquinoline-3-formate, is provided, wherein substituent definitions are as defined in the specification. The preparation method comprises the following steps of: under an acidic condition, dissolving a compound shown as a structural formula III in dimethyl sulfoxide, catalyzing by a ferrous ion (Fe) catalyst, and oxidizing by H2O2 to obtain the 4-hydroxy-1-methyl- 7-phenoxy isoquinoline-3-formate shown as the structuralformula II. By using the method, the production efficiency can be greatly improved, the production cost is reduced, the product purity can be ensured, and the method is suitable for industrial mass production.
4 -HYDROXY- ISOQUINOLINE COMPOUNDS AS HIF HYDROXYLASE INHIBITORS
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, (2013/09/26)
The present invention relates to novel compounds of formula (I), and compositions capable of inhibiting PHD1 enzyme activity selectively over other isoforms, for example, PHD2 and/or PHD3 enzymes. The invention also relates to compounds of formula (I) for use in disorders such as muscle degeneration, colitis, IBD, and certain ischemias.
