100066-86-2 Usage
Molecular structure
1H-Pyrrole-3-carboxylic acid, 2-amino-1-cyclohexyl-4,5-dimethyl-, 1,1-dimethylethyl ester has a complex molecular structure that includes a pyrrole ring, a carboxylic acid group, an amino group, and a 1,1-dimethylethyl ester functional group.
Functional groups
The compound contains several functional groups, including a pyrrole ring, a carboxylic acid group, an amino group, and a 1,1-dimethylethyl ester group.
Methyl groups
The compound has two methyl groups on the cyclohexyl ring, which adds to its complexity.
Potential applications
1H-Pyrrole-3-carboxylic acid, 2-amino-1-cyclohexyl-4,5-dimethyl-, 1,1-dimethylethyl ester may have potential applications in the pharmaceutical industry or in organic synthesis due to its unique structure and functional groups.
Further research
More research is needed to fully understand the properties and potential uses of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 100066-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,0,6 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 100066-86:
(8*1)+(7*0)+(6*0)+(5*0)+(4*6)+(3*6)+(2*8)+(1*6)=72
72 % 10 = 2
So 100066-86-2 is a valid CAS Registry Number.
100066-86-2Relevant articles and documents
Synthesis of 2,7-disubstituted-5,6-dimethylpyrrolo-[2,3-d]-1,3-oxazin-4- ones as antifungal agents
Player,Sowell Sr.
, p. 209 - 214 (2007/10/02)
A series of novel 5,6-dimethylpyrrolo[2,3-d]-1,3-oxazin-4-ones were synthesized from 2-amino-3-tert-butoxy-carbonyl-4,5-dimethylpyrroles. Two methods were used, cyclodehydration of 2-acylamino-3-carboxypyrroles with acetic anhydride and direct conversion of the 5,6-dimethylpyrrolo[2,3-d]- 1,3-oxazin-2,4-diones to the title compounds with an anhydride directly providing the 2 substituent. Molecular modeling techniques revealed that these pyrrolo[2,3-d]oxazinones were rigid analogues of the allylamine antifungals. The compounds were tested for in vitro activity against Tricophyton and Scopulariopsis sp.
