110811-31-9 Usage
General Description
4-Bromo-1-(tert-butoxycarbonyl)-1H-indole-3-carboxylic acid is a chemical compound with a molecular formula C16H16BrNO4. It is a derivative of indole, with a bromine atom and a tert-butoxycarbonyl group attached to the indole ring. 4-BROMO-1-(TERT-BUTOXYCARBONYL)-1H-INDOLE-3-CARBOXYLIC ACID has potential applications in pharmaceutical research and drug development, as indole derivatives are known for their diverse biological activities. The tert-butoxycarbonyl group is commonly used as a protective group in organic synthesis, and the bromine atom can serve as a versatile functional group for further chemical modifications. Further research is needed to explore the specific properties and potential uses of 4-bromo-1-(tert-butoxycarbonyl)-1H-indole-3-carboxylic acid.
Check Digit Verification of cas no
The CAS Registry Mumber 110811-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,8,1 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 110811-31:
(8*1)+(7*1)+(6*0)+(5*8)+(4*1)+(3*1)+(2*3)+(1*1)=69
69 % 10 = 9
So 110811-31-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H6BrNO2/c10-6-2-1-3-7-8(6)5(4-11-7)9(12)13/h1-4,11H,(H,12,13)
110811-31-9Relevant articles and documents
Studies on the Claisen rearrangements in the indolo[2,3-b]quinoline system
Voute, Nicholas,Philp, Douglas,Slawin, Alexandra M. Z.,Westwood, Nicholas J.
supporting information; experimental part, p. 442 - 450 (2010/02/16)
A study of the effect of substrate structure on a Claisen-aza-Cope reaction is presented including a rationalisation of the reaction outcome using DFT calculations. An asymmetric version of the reaction is also described that is of relevance to a proposed
A CONVENIENT SYNTHETIC APPROACH TO 4-SUBSTITUTED INDOLES
Yamada, Fumio,Somei, Masanori
, p. 1173 - 1176 (2007/10/02)
A simple and practical synthetic method for 4-halogenoindoles, 4-indolecarbaldehyde, 4-cyanoindole, and 4-methoxycarbonylindole is elaborated.