23876-07-5 Usage
Uses
Used in Pharmaceutical Industry:
2-(3-amino-2-methylphenyl)acetic acid is utilized as a precursor in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs and medicinal compounds. Its unique structure allows for the creation of molecules with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(3-amino-2-methylphenyl)acetic acid is employed as a precursor in the production of agrochemicals, such as pesticides and herbicides, due to its potential to enhance the effectiveness of these products.
Used in Dye and Pigment Production:
2-(3-amino-2-methylphenyl)acetic acid is used as a building block in the synthesis of dyes and pigments, where its chemical properties contribute to the creation of vibrant and stable colorants for various applications.
Used in Organic Chemistry Research and Development:
2-(3-amino-2-methylphenyl)acetic acid's properties make it suitable for use in research and development within the fields of pharmaceutical and agrochemical industries. It aids in the exploration of new chemical pathways and the discovery of innovative organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 23876-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,7 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23876-07:
(7*2)+(6*3)+(5*8)+(4*7)+(3*6)+(2*0)+(1*7)=125
125 % 10 = 5
So 23876-07-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c1-6-7(5-9(11)12)3-2-4-8(6)10/h2-4H,5,10H2,1H3,(H,11,12)
23876-07-5Relevant academic research and scientific papers
BENZENE COMPOUND HAVING 2 OR MORE SUBSTITUENTS
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, (2008/06/13)
A superior LXR modulator is provided. A compound represented by the general formula (I): [wherein R1: -COR9 (wherein R9: alkyl, optionally substituted alkoxy or optionally substituted amino); R2: H, OH, alkoxy, optionally substituted amino, etc.; R3: H, optionally substituted alkyl, cycloalkyl, optionally substituted alkoxy, optionally substituted amino, halogeno, etc.; R4 and R5: H, optionally substituted alkyl, halogeno, etc.; R6 and R7: H, alkyl; R8: -X2R10 [wherein R10: -COR11 (wherein R11 : OH, optionally substituted alkoxy, optionally substituted amino, etc.), -SO2R12 (wherein R12: optionally substituted alkyl, optionally substituted amino, etc.), tetrazol-5-yl, etc.; X2: single bond, optionally substituted alkylene, etc.]; X1: -NH-, -O-, -S-, etc.; Y1: optionally substituted phenyl, optionally substituted 5- to 6-membered aromatic heterocyclyl; Y2: optionally substituted aryl, optionally substituted heterocyclyl, etc.] and the like is provided.
