86456-12-4 Usage
Appearance
White powder This compound is a white powder, which indicates its physical form and color.
Molecular weight
276.68 g/mol The molecular weight of 2-(3-chlorophenoxy)-5-methoxy-benzoic acid is 276.68 grams per mole, which is the mass of one mole of the compound.
Derivation
Derived from benzoic acid This compound is derived from benzoic acid, which is a simple aromatic carboxylic acid.
Functional groups
Chlorophenoxy and methoxy groups The presence of a chlorophenoxy group (a phenyl ring with a chlorine atom and an ether oxygen) and a methoxy group (an oxygen atom connected to a methyl group) in the structure of this compound.
Uses
Intermediate in organic compound production 2-(3-chlorophenoxy)-5-methoxy-benzoic acid is commonly used as an intermediate in the production of various organic compounds.
Applications
Synthesis of pharmaceuticals and agrochemicals This compound is also used in the synthesis of pharmaceuticals and agrochemicals, which indicates its importance in the development of drugs and chemicals for agricultural purposes.
Unique chemical properties
Due to chlorophenoxy and methoxy groups The presence of the chlorophenoxy and methoxy groups in the structure of 2-(3-chlorophenoxy)-5-methoxy-benzoic acid gives it unique chemical properties, making it valuable for a variety of industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 86456-12-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,5 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86456-12:
(7*8)+(6*6)+(5*4)+(4*5)+(3*6)+(2*1)+(1*2)=154
154 % 10 = 4
So 86456-12-4 is a valid CAS Registry Number.
86456-12-4Relevant articles and documents
Analogues of hycanthone and lucanthone as antitumor agents
Archer,Zayed,Rej,Rugino
, p. 1240 - 1246 (2007/10/02)
Hycanthone analogues (5 and 6) containing 7-substituted hydroxyl groups were prepared and evaluated as antitumor agents. These compounds were significantly more active than the corresponding unsubtituted derivatives. The 7-hydroxylated-4-(hydroxymethyl)-9H-xanthen-9-ones, 11 and 12, were also active antitumor agents. However, the 7-hydroxy-9H-xanthen-9-one counterparts of the 7-hydroxylucanthones were totally devoid of antitumor activity. Results obtained thus far are consistent with the hypothesis that 4-hydroxymethyl substituents in the 9H-xanthen-9-one and 9H-thioxanthen-9-one series are required for antitumor activity.
