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2-methoxy-6-[(phenylamino)methyl]phenol is an organic compound with the molecular formula C15H15NO2. It is a derivative of phenol, featuring a methoxy group at the 2-position and a phenylaminomethyl group at the 6-position. 2-methoxy-6-[(phenylamino)methyl]phenol is characterized by its aromatic structure, with a hydroxyl group and a methoxy group providing it with unique chemical properties. It is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and other organic compounds. presence The of the phenylaminomethyl group suggests potential reactivity in chemical transformations, making it a versatile building block in organic chemistry.

3526-40-7

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3526-40-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3526-40-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,2 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3526-40:
(6*3)+(5*5)+(4*2)+(3*6)+(2*4)+(1*0)=77
77 % 10 = 7
So 3526-40-7 is a valid CAS Registry Number.

3526-40-7Downstream Products

3526-40-7Relevant academic research and scientific papers

Cobalt(II) phthalocyanine-catalyzed highly chemoselective reductive amination of carbonyl compounds in a green solvent

Kumar, Vishal,Sharma, Upendra,Verma, Praveen K.,Kumar, Neeraj,Singh, Bikram

supporting information; experimental part, p. 870 - 878 (2012/05/04)

Cobalt phthalocyanine has been employed for the highly chemoselective reductive amination of aldehydes and ketones in ethanol as a green solvent. A large range of functional groups such as nitro, acid, amide, ester, nitrile, halogen, lactone, methoxy, hydroxy, alkene, N-benzyl, O-benzyl and heterocyclic rings were well tolerated under the present reaction conditions. Copyright

Sulfonic acid supported on hydroxyapatite-encapsulated-γ-Fe 2O3 nanocrystallites as a magnetically separable catalyst for one-pot reductive amination of carbonyl compounds

Deng, Jia,Mo, Li-Ping,Zhao, Fei-Yang,Hou, Lan-Lan,Yang, Li,Zhang, Zhan-Hui

, p. 2576 - 2584 (2011/10/18)

A novel, environmentally friendly procedure has been developed for the preparation of secondary or tertiary amines by one-pot reductive amination of carbonyl compounds using sodium borohydride in the presence of a magnetically recoverable sulfonic acid supported on hydroxyapatite-encapsulated-γ- Fe2O3 [γ-Fe2O3@HAP-SO 3H] at room temperature. The catalyst was easily separated from the reaction mixture by applying an external magnet and reused for six cycles without significant loss of catalytic activity.

Diastereospecific coupling of imines by low-valent titanium: An experimental and Computational study

Kumar, Akshai,Samuelson, Ashoka G.

supporting information; experimental part, p. 951 - 959 (2011/04/15)

The reaction of phenylsilane (PhSiH3) and titanium(IV) isopropoxide [Ti(OiPr)4] generates low-valent titanium alkoxides that reduce and reductively couple imines. The C-C coupling reaction is diastereospecific, with exclusive formati

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