79465-85-3 Usage
Description
(2S)-diMethyl 8-acetyl-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indole-1,2(2H)-dicarboxylate is a synthetic compound characterized by a complex molecular structure. It features two methyl groups, an acetyl group, and two carboxylate groups, all of which contribute to the formation of its tetrahydropyrroloindole ring system. This unique arrangement of functional groups and its tetrahydropyrroloindole framework suggest potential applications in pharmaceuticals or materials science, although further research is required to explore its full potential.
Uses
Used in Pharmaceutical Industry:
(2S)-diMethyl 8-acetyl-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indole-1,2(2H)-dicarboxylate is used as a potential pharmaceutical agent due to its distinctive molecular structure. The presence of multiple functional groups may allow for interactions with biological targets, offering opportunities for the development of new drugs or therapeutic agents.
Used in Materials Science:
In the field of materials science, (2S)-diMethyl 8-acetyl-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indole-1,2(2H)-dicarboxylate may be utilized for the development of novel materials with specific properties. Its unique structure could contribute to the creation of new polymers, coatings, or other advanced materials with tailored characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 79465-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,6 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79465-85:
(7*7)+(6*9)+(5*4)+(4*6)+(3*5)+(2*8)+(1*5)=183
183 % 10 = 3
So 79465-85-3 is a valid CAS Registry Number.
79465-85-3Relevant articles and documents
Synthesis of potent BCRP inhibitor-Ko143
Li, Yuexian,Hayman, Erik,Plesescu, Mihaela,Prakash, Shimoga R.
, p. 1480 - 1483 (2008/09/18)
Two routes for the synthesis of potent BCRP inhibitor-Ko143 are reported. The key intermediate, 6-methoxytryptophan derivative, was synthesized by an improved procedure, ytterbium triflate-promoted coupling between 6-methoxyindole and optically active 1-b
Synthesis of 5-cyano-I-tryptophan
Dua, Rajesh K.,Phillips, Robert S.
, p. 29 - 32 (2007/10/02)
The 5-bromo derivative 2 of the cyclic tautomer of Nb-methoxycarbonyl-L-tryptophan methyl ester 1 undergoes reaction with CuCN in refluxing N-methylpyrrolidone (NMP) to give 5-cyano derivative 3a with some ring opened 5-cyano product 3b. Both 3a and 3b can be converted, in high yield, into free 5-cyano-L-tryptophan 4 with BBr3 under mild conditions.