127817-85-0 Usage
Description
4-Methoxy-2-(trifluoromethyl)benzoic acid is an organic compound characterized by its white powder form. It features a benzoic acid structure with a methoxy group at the 4-position and a trifluoromethyl group at the 2-position, which may contribute to its unique chemical properties and reactivity.
Uses
Used in Pharmaceutical Industry:
4-Methoxy-2-(trifluoromethyl)benzoic acid is used as a reactant for the synthesis of phenothiazines, which are a class of chemical compounds that include various drugs with a wide range of applications, particularly in the treatment of psychiatric disorders such as schizophrenia and bipolar disorder. The unique structure of 4-Methoxy-2-(trifluoromethyl)benzoic acid allows for the creation of phenothiazine derivatives with potentially improved pharmacological properties.
Used in Chemical Synthesis:
In the field of organic chemistry, 4-Methoxy-2-(trifluoromethyl)benzoic acid can be utilized as a building block or intermediate for the synthesis of various other complex organic molecules. Its specific functional groups and trifluoromethyl substitution may offer advantages in the development of novel compounds with tailored properties for different applications, such as agrochemicals, dyes, or advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 127817-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,8,1 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 127817-85:
(8*1)+(7*2)+(6*7)+(5*8)+(4*1)+(3*7)+(2*8)+(1*5)=150
150 % 10 = 0
So 127817-85-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F3O3/c1-15-5-2-3-6(8(13)14)7(4-5)9(10,11)12/h2-4H,1H3,(H,13,14)
127817-85-0Relevant articles and documents
2-trifluoromethyl-4-hydroxybenzoic acid
-
, (2008/06/13)
Disclosed is a novel compound 2-trifluoromethyl-4-hydroxybenzoic acid represented by the formula: STR1
Antiestrogenic N-(4-hydroxyphenyl)-N-(1,1,1-trifluoro-2-propyl)-4-hydroxybenzamides: Influence of hydrophobic groups substituted in the ortho-position of the benzamide-fragment on activity
Hartmann,Vom Orde,Schonenberger
, p. 73 - 78 (2007/10/02)
Experiments are reported here to develop compounds with antiestrogenic and mammary tumor inhibiting properties. Analogues with hydrophobic groups in 2- or 2,6-position of the benzamide-fragment of N-(4-hydroxyphenyl)-N-(1,1,1-trifluoro-2-propyl)-4-hydroxy
