32338-02-6 Usage
Description
2-BROMO-4-METHOXY-PHENYLAMINE is an organic compound that serves as a reagent and reactant in various chemical reactions, particularly in organometallics and organic synthesis. Its unique structure, featuring a bromo and methoxy group attached to an aniline, makes it a versatile building block for the development of new compounds and materials.
Uses
Used in Organometallic Chemistry:
2-BROMO-4-METHOXY-PHENYLAMINE is used as a reagent in organometallic chemistry for the synthesis of metal complexes and coordination compounds. Its presence in these reactions allows for the formation of stable complexes with specific properties, which can be utilized in various applications, such as catalysis, materials science, and pharmaceuticals.
Used in Organic Synthesis:
In the field of organic synthesis, 2-BROMO-4-METHOXY-PHENYLAMINE is employed as a reactant for the preparation of a wide range of organic compounds. Its functional groups can be selectively modified or used as starting points for the formation of new chemical bonds, enabling the synthesis of complex molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
2-BROMO-4-METHOXY-PHENYLAMINE is used as a building block in the pharmaceutical industry for the development of new drugs and drug candidates. Its unique structure can be incorporated into drug molecules to impart specific biological activities, such as binding to target proteins or enzymes, modulating cellular pathways, or exhibiting therapeutic effects.
Used in Materials Science:
In materials science, 2-BROMO-4-METHOXY-PHENYLAMINE is utilized as a component in the design and synthesis of new materials with tailored properties. Its incorporation into polymers, coatings, or other materials can result in improved performance, such as enhanced stability, increased reactivity, or specific optical, electronic, or mechanical properties.
Overall, 2-BROMO-4-METHOXY-PHENYLAMINE is a valuable compound in the fields of organometallic chemistry, organic synthesis, pharmaceuticals, and materials science, offering a wide range of applications and potential for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 32338-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,3 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 32338-02:
(7*3)+(6*2)+(5*3)+(4*3)+(3*8)+(2*0)+(1*2)=86
86 % 10 = 6
So 32338-02-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H8BrNO/c1-10-5-2-3-7(9)6(8)4-5/h2-4H,9H2,1H3
32338-02-6Relevant articles and documents
An easy and efficient access to 2-bromo-4-methoxyaniline
Cossy,Poitevin,Pardo, D. Gomez,Peglion
, p. 3525 - 3527 (1997)
2-Bromo-4-methoxyaniline was obtained by treatment of 2,6-dibromo-4-methoxyaniline with n-butyllithium.
Methoxy aniline compound and synthesis method thereof
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Paragraph 0027; 0030-0032; 0041-0042, (2021/05/19)
The invention mainly relates to a preparation method of anisidine. According to the technical scheme, under the promotion of the photocatalyst and blue light, in the argon atmosphere, nitro compounds and methanol generate methoxyaniline, wherein products and additional products with stable molecular structures and excellent chemical properties are prepared, wherein a photocatalyst and a blue light source are used in the method, and a new path is provided for synthesis of methoxyaniline compounds. The method has the characteristics of mild reaction conditions, simple reaction system, less reaction equipment, simplicity and convenience in experimental operation and the like. The methoxyaniline derivative and the synthetic method thereof can be applied to a plurality of industrial production fields of dyes, pesticides, medicines, rubber additives and the like. The method is particularly suitable for scientific research, development and utilization of efficient and selective synthesis of methoxyaniline compounds by a one-pot method.
COMPOUNDS AND METHODS FOR TREATMENT OF HEDGEHOG PATHWAY ASSOCIATED CONDITIONS
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Page/Page column 78; 80; 81, (2020/01/24)
Provided herein is novel compounds of formula (I), (II), (III), (IV), and (V) as described in the specification, and pharmaceutically acceptable salts, solvates, and prodrugs and compositions thereof, and methods of measuring hedgehog pathway activation in tumor cells, examining tumor cell proliferation, differentiation and apoptosis and using the compounds and pharmaceutical compositions disclosed for treatment of diseases and disorders associated with the hedgehog signaling pathway.
