5653-46-3 Usage
General Description
2-Hydroxy-3,4-dimethoxybenzoic acid is an organic compound that falls under the class of phenolic acids and derivatives. These are compounds containing a phenolic ring, which is a benzene ring with one hydroxyl group. 2-HYDROXY-3,4-DIMETHOXYBENZOIC ACID, in particular, possesses three functional groups; two methoxy groups at positions 3 and 4, and a carboxylic acid group. Its chemical structure is characterized by two methoxy groups (-O-CH3) attached to the phenyl ring, along with a carboxylic acid group (-COOH) and a hydroxyl (-OH) group. Its applications and uses have not been reported and it has not been classified for hazards according to GHS (Globally Harmonized System of Classification and Labelling of Chemicals) standards.
Check Digit Verification of cas no
The CAS Registry Mumber 5653-46-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5653-46:
(6*5)+(5*6)+(4*5)+(3*3)+(2*4)+(1*6)=103
103 % 10 = 3
So 5653-46-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O5/c1-13-6-4-3-5(9(11)12)7(10)8(6)14-2/h3-4,10H,1-2H3,(H,11,12)
5653-46-3Relevant articles and documents
Govindachari et al.
, p. 243,248 (1967)
COMPOUNDS FOR THE TREATMENT OF PARAMOXYVIRUS VIRAL INFECTIONS
-
Paragraph 0408, (2014/03/25)
Disclosed herein are new antiviral compounds, together with pharmaceutical compositions that include one or more antiviral compounds, and methods of synthesizing the same. Also disclosed herein are methods of ameliorating and/or treating a paramyxovirus viral infection with one or more small molecule compounds. Examples of paramyxovirus infection include an infection caused by human respiratory syncytial virus (RSV).
Competition of substituents for ortho direction of metalation of veratric acid
Chau, Nguyet Trang Thanh,Nguyen, Thi Huu,Castanet, Anne-Sophie,Nguyen, Kim Phi Phung,Mortier, Jacques
, p. 10552 - 10557 (2008/12/23)
LTMP (5 equiv) metalates randomly veratric acid (1). Under external quench conditions, the thermodynamically more stable lithium 2-lithio-3,4-dimethoxybenzoate (2) reacts with a variety of electrophiles to give versatile building units that are not easily accessible by conventional means. Under in situ quench conditions (LTMP/TMSCl), a reversal of regioselectivity is observed and 6-trimethylsilyl-3,4-dimethoxybenzoic acid (10) is formed predominantly.
