929098-68-0 Usage
Molecular structure
1H,3H-Pyrrolo[1,2-c]thiazole-6,7-dicarboxylic acid, 1,1,5-trimethyl-3-phenyl-, 6,7-dimethyl ester is a complex organic compound that features a pyrrolo-thiazole ring structure with two carboxylic acid groups, a methyl group, and a phenyl group attached.
Ester groups
The compound contains two ester groups, which are formed when the carboxylic acids react with alcohols. This gives the compound a unique chemical structure and properties.
Biological activity
The pyrrolo-thiazole ring structure found in 1H,3H-Pyrrolo[1,2-c]thiazole-6,7-dicarboxylic acid,
1,1,5-trimethyl-3-phenyl-, 6,7-dimethyl ester is present in some biologically active compounds, suggesting that it may have potential applications in pharmaceuticals.
Building block in organic synthesis
The multiple functional groups in the compound make it a potentially useful building block in organic synthesis, allowing for the creation of a variety of new compounds with different properties and applications.
Further research needed
To fully understand the properties and potential uses of 1H,3H-Pyrrolo[1,2-c]thiazole-6,7-dicarboxylic acid,
1,1,5-trimethyl-3-phenyl-, 6,7-dimethyl ester, additional research and testing would be required. This may include studying its chemical reactivity, stability, and potential interactions with other compounds or biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 929098-68-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,0,9 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 929098-68:
(8*9)+(7*2)+(6*9)+(5*0)+(4*9)+(3*8)+(2*6)+(1*8)=220
220 % 10 = 0
So 929098-68-0 is a valid CAS Registry Number.
929098-68-0Relevant academic research and scientific papers
Pinho e Melo, Teresa M.V.D.,Soares, Maria I.L.,Nunes, Cláudio M.
, p. 1833 - 1841 (2007)
Azafulvenium methides generated by the thermal extrusion of SO2 from 1-methyl- and 1,1-dimethyl-1H,3H-pyrrolo[1,2-c]thiazole-2,2-dioxides undergo [1,8]H sigmatropic shifts to give vinylpyrroles. Flash vacuum pyrolysis of the C-vinylpyrroles affords 5-oxo-5H-pyrrolizines or C-allyl-1H-pyrroles.
