130662-48-5 Usage
Aromatic Compound
Yes
Explanation
Aromatic compounds are characterized by a ring of carbon atoms with delocalized electrons, which gives them a distinct stability and reactivity. This compound has a benzene ring, making it an aromatic compound.
Explanation
The presence of a bromine (Br) atom and a methoxy (-OCH3) group attached to the benzene ring provides unique chemical properties and reactivity to the compound.
Explanation
This compound serves as a starting material for the synthesis of more complex organic molecules, which can be used in various applications, including pharmaceuticals and agrochemicals.
Explanation
The compound has been studied for its potential biological activities, such as anti-inflammatory and antioxidant effects, which could lead to its use in the development of new drugs.
Explanation
As a precursor, this compound is used to synthesize other chemicals that are used in the production of pharmaceuticals and agrochemicals, which are essential for various industries.
Explanation
The structure of the compound is defined by its specific arrangement of atoms and functional groups. In this case, the compound has an isobenzofuranone core with a bromine atom at the 4-position and a methoxy group at the 7-position.
Bromo and Methoxy Groups
Attached to the benzene ring
Use in Organic Synthesis
Building block for complex molecules
Pharmaceutical Research
Potential biological activities and medicinal properties
Precursor in Production
Pharmaceuticals and agrochemicals
Structure
1(3H)-Isobenzofuranone, 4-bromo-7-methoxy-
Check Digit Verification of cas no
The CAS Registry Mumber 130662-48-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,6 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 130662-48:
(8*1)+(7*3)+(6*0)+(5*6)+(4*6)+(3*2)+(2*4)+(1*8)=105
105 % 10 = 5
So 130662-48-5 is a valid CAS Registry Number.
130662-48-5Relevant articles and documents
A New Synthetic Route to 4-Bromo-7-methoxyphthalide and 3-Hydroxy-7-methoxyphthalide from 2-Methoxy-6-methylbenzoate Side Chain and Nuclear Bromination
Islam, Md. Rabiul,Joule, John A.
, p. 367 - 378 (2007/10/02)
Ethyl 2-methoxy-6-methylbenzoate was converted via its acid and acid chloride, into the methyl ester.Bromination of the methyl and ethyl esters with the halogen in carbon tetrachloride at reflux in the presence of light resulted in both side-chain and nuc
