6742-29-6 Usage
Bicyclic organic compound
Indene-based structure The compound has a bicyclic (two interconnected rings) structure derived from indene, which is a type of aromatic hydrocarbon.
Carboxylic acid derivative
Contains a carboxyl functional group The molecule has a carboxyl group (-COOH) attached to the bicyclic structure, making it an acidic compound.
Ketone group
1-oxo (one oxygen atom double-bonded to a carbon) The presence of a ketone group in the structure indicates that the compound has potential reactivity in various chemical reactions.
Potential applications
Organic synthesis, pharmaceuticals, and industrial processes This chemical may be useful in the synthesis of other organic compounds, as well as in the development of pharmaceutical drugs and various industrial applications.
Safety precautions
Handle with care and follow proper safety measures Due to the potential hazards associated with this compound, it is important to handle it with care and follow appropriate safety guidelines to minimize risks.
Check Digit Verification of cas no
The CAS Registry Mumber 6742-29-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,4 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6742-29:
(6*6)+(5*7)+(4*4)+(3*2)+(2*2)+(1*9)=106
106 % 10 = 6
So 6742-29-6 is a valid CAS Registry Number.
6742-29-6Relevant articles and documents
Regioselectivity of Radical-induced Bond Cleavages in Epoxides
Murphy, John A.,Patterson, Christopher W.
, p. 405 - 410 (2007/10/02)
Radical-induced carbon-carbon and carbon-oxygen bond cleavage reactions in a highly substituted epoxide, and in epoxides fused to other rings are reported.Substitution at the site of the developing radical assists C-C bond cleavage.In ring-fused epoxides, C-C bond cleavage was not seen where stereoelectronic factors oppose it.
