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16495-67-3

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16495-67-3 Usage

General Description

The chemical ISOPROPYL-(4-METHOXY-PHENYL)-AMINE, also known as 4-Methoxyphenylisopropylamine, is an organic compound with the molecular formula C10H15NO. This chemical belongs to the group of amines and is commonly used as an intermediate for the synthesis of various pharmaceuticals and organic compounds. It is a colorless liquid with a slightly amine-like odor and is soluble in most organic solvents. ISOPROPYL-(4-METHOXY-PHENYL)-AMINE is known for its role as a building block in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, it is used in the manufacture of dyes, flavors, and fragrances.

Check Digit Verification of cas no

The CAS Registry Mumber 16495-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,9 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16495-67:
(7*1)+(6*6)+(5*4)+(4*9)+(3*5)+(2*6)+(1*7)=133
133 % 10 = 3
So 16495-67-3 is a valid CAS Registry Number.

16495-67-3Relevant articles and documents

Tris(pyrazolyl)borate rhodium complexes. Application for reductive amination and esterification of aldehydes in the presence of carbon monoxide

Kharitonov, Vladimir B.,Ostrovskii, Vladimir S.,Nelyubina, Yulia V.,Muratov, Dmitry V.,Chusov, Denis,Loginov, Dmitry A.

, (2020)

The halide complexes TpRhCl2(MeOH) and TpMe2RhI2(CO) (Tp = hydrotris-(pyrazolyl)borate; TpMe2 = hydrotris-(3,5-dimethylpyrazolyl)borate) were synthesized by reactions of RhCl3 with K[Tp] in methanol and TpMe2Rh(CO)2 with iodine, respectively. Reactions of TpMe2RhCl2(MeOH) and TpMe2RhI2(CO) with 1,10-phenanthroline afford the phenanthroline derivatives [TpMe2Rh(phen)X]+ (X = Cl, I). The structures of TpRhCl2(MeOH) and TpRhI2(CO) were determined by X-ray diffraction. Tris(pyrazolyl)borate rhodium complexes effectively catalyze the reductive amination and the reductive esterification of aldehydes in the presence of carbon monoxide.

Enhancing the efficiency of the ruthenium catalysts in the reductive amination without an external hydrogen source

Afanasyev, Oleg I.,Chusov, Denis,Fatkulin, Artemy R.,Tsygankov, Alexey A.

, p. 404 - 409 (2022/01/13)

Catalytic reductive reactions are essential for laboratory and industrial-scale organic synthesis. However, the nowadays trend is the development of new, progressively more complicated reducing systems, which hinders the application of such highly efficie

Easy Access to Versatile Catalytic Systems for C?H Activation and Reductive Amination Based on Tetrahydrofluorenyl Rhodium(III) Complexes

Kharitonov, Vladimir B.,Runikhina, Sofiya A.,Nelyubina, Yulia V.,Muratov, Dmitry V.,Chusov, Denis,Loginov, Dmitry A.

supporting information, p. 10903 - 10912 (2021/06/28)

On the basis of the 1,2,3,4-tetrahydrofluorenyl ligand, a simple approach was developed to new effective rhodium catalysts for the construction of C?C and C?N bonds. The halide compounds [(η5-tetrahydrofluorenyl)RhX2]2 (2

Alkyl formates as reagents for reductive amination of carbonyl compounds

Afanasyev, Oleg I.,Cherkashchenko, Ilia,Kuznetsov, Anton,Kliuev, Fedor,Semenov, Sergey,Chusova, Olga,Denisov, Gleb,Chusov, Denis

, p. 112 - 113 (2020/03/03)

Alkyl formates in the presence of basic additives can serve as a reagent in the direct reductive amination of carbonyl compounds. The developed procedure can be applied to various aldehydes and ketones with electron donating and electron withdrawing groups.

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