7269-72-9 Usage
Indole derivative
Aldehyde derivative of indole This compound is derived from the indole structure, with an aldehyde functional group (-CHO) attached to the third carbon of the indole ring.
Synthetic intermediate
Used in the production of pharmaceuticals, dyes, and fragrances 1H-Indole-3-acetaldehyde, a-oxois commonly used as a building block in the synthesis of various pharmaceuticals, dyes, and fragrances due to its reactive nature and versatility.
Biological activities
Potential anti-inflammatory and anticancer properties Studies have shown that this compound may serve as a precursor for the synthesis of novel indole derivatives with potential anti-inflammatory and anticancer activities.
Organic synthesis
Versatile building block for complex molecules 1H-Indole-3-acetaldehyde, a-oxohas been investigated for its potential use in organic synthesis as a versatile building block, allowing for the construction of complex molecular structures.
Significant role in organic chemistry
Wide range of potential applications This compound plays an important role in organic chemistry, with a broad range of potential applications in various industries, including pharmaceuticals, dyes, and fragrances.
Check Digit Verification of cas no
The CAS Registry Mumber 7269-72-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,6 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7269-72:
(6*7)+(5*2)+(4*6)+(3*9)+(2*7)+(1*2)=119
119 % 10 = 9
So 7269-72-9 is a valid CAS Registry Number.
7269-72-9Relevant articles and documents
Radical Chain Reaction or Benzenethiol with Pentynylthiol Esters: Production of Aldehydes under Stannane/Silane-Free Conditions
Benati, Luisa,Leardini, Rino,Minozzi, Matteo,Nanni, Daniele,Scialpi, Rosanna,Spagnolo, Piero,Zanardi, Giuseppe
, p. 985 - 990 (2007/10/03)
The radical chain reaction of benzenethiol with accessible 4-pentynylthiol esters provides a new stannane/silane-free protocol for the production of aromatic and aliphatic aldehydes. The procedure is especially useful for the aryl and primary aldehydes, even in the presence of substituents highly sensitive to reductive conditions, and is also of some utility for the vinylic and secondary ones, The protocol is instead not applicable to the tertiary aldehydes, owing to preferential alkane-forming decarbonylation, although the tertiary ones derived from bridgehead precursors can still be usefully produced.
