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4-(1-Methyl-5-imidazolyl)aniline, also known as N-(1-methyl-5-imidazolyl)-4-aminobenzene, is a chemical compound that belongs to the class of aromatic amines. It has a molecular formula of C10H11N3 and a molecular weight of 161.21 g/mol. This pale yellow solid at room temperature is sparingly soluble in water and is known for its potential biological and pharmacological activities, as well as its use in various applications such as a pharmaceutical intermediate and a reagent in organic synthesis.

89250-15-7

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89250-15-7 Usage

Uses

Used in Pharmaceutical Industry:
4-(1-Methyl-5-iMidazolyl)aniline is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique chemical structure allows it to be a key component in the development of new medications with potential therapeutic benefits.
Used in Organic Synthesis:
In the field of organic synthesis, 4-(1-Methyl-5-iMidazolyl)aniline serves as a reagent, contributing to the formation of complex organic compounds. Its presence in reactions can facilitate the synthesis of desired products, making it a valuable tool for chemists.
Used in Research and Development:
4-(1-Methyl-5-iMidazolyl)aniline is utilized in research and development for exploring its potential biological and pharmacological activities. Studies on 4-(1-Methyl-5-iMidazolyl)aniline can lead to a better understanding of its properties and applications, paving the way for new discoveries and innovations in the scientific community.

Check Digit Verification of cas no

The CAS Registry Mumber 89250-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,5 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89250-15:
(7*8)+(6*9)+(5*2)+(4*5)+(3*0)+(2*1)+(1*5)=147
147 % 10 = 7
So 89250-15-7 is a valid CAS Registry Number.

89250-15-7Relevant academic research and scientific papers

HYDRAZONE DERIVATIVE

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Page/Page column 29, (2010/11/08)

A compound represented by the following formula (I): wherein R1 represents hydrogen, aryl which may have a substituent, a saturated or unsaturated 5- to 7-membered heterocyclic group which may have a substituent, etc.; R2 represents hydrogen, aryl which may have a substituent, a saturated or unsaturated 5- to 7-membered heterocyclic group which may have a substituent, etc.; R3 represents hydrogen, etc.; Ar represents a divalent group derived from aromatic hydrocarbon, etc.; X represents a single bond, linear or branched alkylene having from 1 to 3 carbon atoms which may have a substituent, etc.; and G represents halogen, a saturated or unsaturated 5- or 6-membered cyclic hydrocarbon group which may have a substituent, a saturated or unsaturated 5- to 7-membered heterocyclic group which may have a substituent, etc., a salt thereof or a solvate thereof; and an agent for inhibiting aggregation and/or deposition of an amyloid protein or an amyloid-like protein, which comprises the compound, a salt thereof or a solvate thereof

Ionization, tautomerism and molecular conformation in aqueous solution of the histamine H2-receptor antagonist mifentidine

Bazzano,Vavoni,Mondoni,et al.

, p. 27 - 33 (2007/10/02)

Ionization (pK(a)) and tautomeric (K(t)) constants of mifentidine (DA4577) have been determined in aqueous solution. The predominant molecular species at physiological pH (7.4) is the monocationic form (95.3%) at the formamidine moiety, with the imidazole

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