51971-09-6 Usage
General Description
2,6-dimethoxy-9H-carbazole-3-carbaldehyde is a chemical compound with the molecular formula C15H13NO3. It is a derivative of carbazole, a common organic compound found in various natural products and existing in numerous synthetic compounds. This specific derivative contains two methoxy groups and an aldehyde functional group on the carbazole ring. It is often used in organic synthesis and medicinal chemistry as a building block or intermediate for the preparation of other compounds. The aldehyde group makes it a versatile starting material for the synthesis of various aromatic and heterocyclic compounds with potential pharmaceutical applications. Additionally, its carbazole backbone gives it interesting electronic and photochemical properties, making it a potential candidate for optoelectronic devices and organic light-emitting diodes (OLEDs).
Check Digit Verification of cas no
The CAS Registry Mumber 51971-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,7 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51971-09:
(7*5)+(6*1)+(5*9)+(4*7)+(3*1)+(2*0)+(1*9)=126
126 % 10 = 6
So 51971-09-6 is a valid CAS Registry Number.
51971-09-6Relevant articles and documents
C-N bond formation via Cu-catalyzed cross-coupling with boronic acids leading to methyl carbazole-3-carboxylate: Synthesis of carbazole alkaloids
Rasheed, Sk.,Rao, D. Nageswar,Reddy, K. Ranjith,Aravinda,Vishwakarma, Ram A.,Das, Parthasarathi
, p. 4960 - 4969 (2014/01/23)
Copper promoted N-arylation of methyl 4-amino-3-iodobenzoate with boronic acids followed by Pd-catalyzed intramolecular C-H arylation provides an efficient route to methyl carbazole-3-carboxylate derivatives. This methodology was implemented in the synthe
Elvirol Methyl Ether: A New Synthesis and niogenetic Proposal
Pednekar, P. R.,Chakravarti, K. K.,Paknikar, S. K.
, p. 1076 - 1077 (2007/10/02)
A new synthesis of elvirol methyl ether (1b) is described.It is suggested that elvirol (1a) may arise biogenetically via a pinacolic rearrangement of a glycol, derived from an arene oxide intermediate.
