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N-(3,4-dihydro-1H-imidazol-2-yl)-aminomethyl benzene hydroiodide is a complex organic compound with the chemical formula C9H12N3I. It is a derivative of benzene, featuring an imidazole ring attached to the aminomethyl group. N-(3,4-dihydro-1H-imidazol-2-yl)-aminomethyl benzene hydroiodide is characterized by its hydroiodide salt form, indicating the presence of iodide ions (I-). It is often used in chemical research and synthesis due to its unique structure and reactivity. The compound's properties, such as solubility and stability, can be influenced by the presence of the hydroiodide salt, making it a potentially useful intermediate in the preparation of various pharmaceuticals and other chemical products.

6182-02-1

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6182-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6182-02-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,8 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6182-02:
(6*6)+(5*1)+(4*8)+(3*2)+(2*0)+(1*2)=81
81 % 10 = 1
So 6182-02-1 is a valid CAS Registry Number.

6182-02-1Downstream Products

6182-02-1Relevant academic research and scientific papers

Calorimetric investigation of guanidinium-carboxylate interactions

Linton, Brian,Hamilton, Andrew D.

, p. 6027 - 6038 (1999)

Isothermal titration calorimetry was utilized to study the association between a series of guanidinium derivatives and tetrabutylammonium acetate. This technique provides a measure of association strength, stoichiometry of binding, as well as thermodynami

Tandem copper catalyzed regioselectiveN-arylation-amidation: synthesis of angularly fused dihydroimidazoquinazolinones and the anticancer agent TIC10/ONC201

Honnanayakanavar, Jyoti M.,Nanubolu, Jagadeesh Babu,Suresh, Surisetti

supporting information, p. 8497 - 8501 (2021/10/20)

Herein, we present a copper-catalyzed tandem reaction of 2-aminoimidazolines andortho-halo(hetero)aryl carboxylic acids that causes the regioselective formation of angularly fused tricyclic 1,2-dihydroimidazo[1,2-a]quinazolin-5(4H)-one derivatives. The reaction involved in the construction of the core six-membered pyrimidone moiety proceededviaregioselectiveN-arylation-condensation. The presented protocol been successfully applied to accomplish the total synthesis of TIC10/ONC201, which is an active angular isomer acting as a tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL): a sought after anticancer clinical agent.

Microwave-induced synthesis of 2-aminoimidazolines under neat conditions

Genc, Murat,Servi, Sueleyman

experimental part, p. 3263 - 3277 (2011/03/18)

2-Aminoimidazolines were synthesized by the nucleophilic substitution reaction of 2-methylmercapto-4,5-dihydroimidazole hydroiodide with various amine compounds under neat conditions. Copyright Taylor & Francis Group, LLC.

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