126503-08-0 Usage
Molecular Structure
A complex structure consisting of a spiro ring system with a dioxa (two oxygen atoms) and an aza (one nitrogen atom) bridge, a carboxylic acid group, a methyl group at the 7th position, and a 1,1-dimethylethyl ester group.
Functional Groups
Carboxylic acid, ester, and methyl groups.
Ester Formation
The compound is formed by the reaction of the carboxylic acid group with an alcohol, specifically 1,1-dimethylethyl alcohol, resulting in an ester linkage.
Derivative
It is a derivative of 1,4-dioxaspiro[4.5]decane, with additional functional groups attached.
Applications
Likely used in chemical research and development, and may have potential applications in pharmaceuticals or materials science due to its unique structure.
Complexity
The presence of the 1,1-dimethylethyl group adds to the complexity of the compound, making it a more intricate molecule.
Stereochemistry
The stereochemistry of the molecule is not explicitly mentioned, but it is important to consider the arrangement of atoms in three-dimensional space when studying its properties and potential applications.
Solubility
The solubility of this compound is not provided, but it can be inferred that it may be soluble in organic solvents due to the presence of the ester and methyl groups.
Check Digit Verification of cas no
The CAS Registry Mumber 126503-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,5,0 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 126503-08:
(8*1)+(7*2)+(6*6)+(5*5)+(4*0)+(3*3)+(2*0)+(1*8)=100
100 % 10 = 0
So 126503-08-0 is a valid CAS Registry Number.
126503-08-0Relevant articles and documents
BENZAMIDINE DERIVATIVE
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Page 153, (2010/02/05)
Compounds of general formula (1) and pharmacologically acceptable salts thereof: ???[wherein ??????R1 represents a hydrogen atom, a halogen atom, an alkyl group or a hydroxyl group; ??????R2 represents a hydrogen atom or a halogen atom; ??????R3 represents a hydrogen atom, an alkyl group which may be substituted, an aralkyl group, an alkylcarbonyl group which may be substituted, an alkylsulfonyl group which may be substituted or the like; ??????each of R4 and R5 represents a hydrogen atom, a halogen atom, an alkyl group which may be substituted, a carbamoyl group or the like; ??????R6 represents a heterocycle or the like; ??????each of R7 and R8 represents a hydrogen atom, an alkyl group or the like; ??????n represents 0, 1 or 2] ???exhibit excellent activated blood coagulation factor X inhibitory activity and are useful for the prevention or treatment of blood coagulation-related diseases.
α-Lithioamine Synthetic Equivalents: Syntheses of Diastereoisomers from the Boc Piperidines
Beak, Peter,Lee, Won Koo
, p. 2578 - 2580 (2007/10/02)
The α'-lithiations and electrophilic substitutions of selected Boc piperidines provide single or separable diastereoisomeric 2-substituted, 2,4-disubstituted, and 2,4,6-trisubstituted Boc piperidines which are readily hydrolyzed to the substituted piperidines.
