134822-76-7 Usage
Uses
Used in Pharmaceutical Industry:
6-Hydroxychromene-3-carboxaldehyde is utilized as a key intermediate in the synthesis of pharmaceuticals for its potential biological activities. Its antioxidant properties make it a candidate for the development of drugs targeting conditions associated with oxidative stress, while its antibacterial and antifungal activities suggest its use in treatments for infectious diseases.
Used in Organic Synthesis:
In the field of organic synthesis, 6-Hydroxychromene-3-carboxaldehyde is employed as a building block for creating diverse organic compounds. Its unique structure allows for various chemical reactions, facilitating the production of new molecules with potential applications in different industries.
Used in Medicinal Chemistry Research:
6-Hydroxychromene-3-carboxaldehyde is used as a subject of study in medicinal chemistry to explore its potential as a therapeutic agent. Researchers are interested in its biological activities and how these can be harnessed to develop new drugs with improved efficacy and safety profiles.
Used in the Development of Functional Materials:
Due to its reactivity and structural features, 6-Hydroxychromene-3-carboxaldehyde is also used in the creation of functional materials with specific properties, such as those needed in sensors, catalysts, or other advanced materials with specialized applications.
Check Digit Verification of cas no
The CAS Registry Mumber 134822-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,2 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 134822-76:
(8*1)+(7*3)+(6*4)+(5*8)+(4*2)+(3*2)+(2*7)+(1*6)=127
127 % 10 = 7
So 134822-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H8O3/c11-5-7-3-8-4-9(12)1-2-10(8)13-6-7/h1-5,12H,6H2
134822-76-7Relevant articles and documents
Substituted heterocyclic compounds, method for preparing and compositions containing same
-
, (2008/06/13)
The invention relates to compounds of formula (I): wherein: R1, R2and R3are as defined in the description, X is as defined in the description, Y represents an oxygen atom, a sulphur atom, a C(H)qgroup, SO or SO2, n is equal to from 0 to 5, A represents a NR5R6group, and medicinal products containing the same which are useful in treating or in preventing melatoninergic disorders.
Substituted chromenes as potent, orally active 5-lipoxygenase inhibitors
Satoh,Stanton,Hutchison,Libby,Kowalski,Lee,White,Kimble
, p. 3580 - 3594 (2007/10/02)
A series of chromene derivatives was synthesized and evaluated for their in vitro and ex vivo 5-lipoxygenase (5-LO) inhibitory activity. These compounds were prepared by condensation of appropriate salicyl aldehydes with α,β-unsaturated carbonyl compounds
CERTAIN BENZOPYRAN AND BENZOTHIOPYRAN DERIVATIVES
-
, (2008/06/13)
The invention relates to the compounds of the formula wherein each R independently represents hydrogen, lower alkyl, halogen, trifluoromethyl, lower alkoxy, carbocyclic or heterocyclic aryl, carbocyclic or heterocyclic aryloxy, carbocyclic or heterocyclic
