100066-79-3 Usage
Uses
Used in Organic Chemistry:
1-BENZYL-2-AMINO-3-TERT-BUTOXYCARBONYL-4,5-DIMETHYLPYRROLE is used as a building block for the synthesis of various heterocyclic compounds due to its structural complexity and the presence of multiple functional groups that can be further modified in chemical reactions.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 1-BENZYL-2-AMINO-3-TERT-BUTOXYCARBONYL-4,5-DIMETHYLPYRROLE is used as an intermediate for the preparation of pharmaceuticals. Its versatility allows for the development of molecules with potential therapeutic applications, taking advantage of the compound's ability to be incorporated into complex organic structures.
Used in the Synthesis of Biologically Active Molecules:
1-BENZYL-2-AMINO-3-TERT-BUTOXYCARBONYL-4,5-DIMETHYLPYRROLE is utilized as a key intermediate in the creation of biologically active molecules. The presence of the amino and tert-butoxycarbonyl groups provides opportunities for the attachment of various functional groups, enhancing the compound's potential for interaction with biological targets.
Used in the Protection of Amino Groups:
During the synthesis of complex organic molecules, the benzyl group in 1-BENZYL-2-AMINO-3-TERT-BUTOXYCARBONYL-4,5-DIMETHYLPYRROLE serves to protect the amino group, preventing unwanted side reactions and ensuring the successful construction of the desired molecular architecture. This protective feature is particularly valuable in multi-step organic synthesis processes.
Check Digit Verification of cas no
The CAS Registry Mumber 100066-79-3 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, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100066-79:
(8*1)+(7*0)+(6*0)+(5*0)+(4*6)+(3*6)+(2*7)+(1*9)=73
73 % 10 = 3
So 100066-79-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H24N2O2/c1-12-13(2)20(11-14-9-7-6-8-10-14)16(19)15(12)17(21)22-18(3,4)5/h6-10H,11,19H2,1-5H3
100066-79-3Relevant academic research and scientific papers
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.
