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1-[2-(N,N-dimethylaminomethyl)ferrocenyl]-1,1-diphenylmethanol is a complex organic compound that features a unique structure. At its core, it contains a ferrocene unit, which is a sandwich-type complex with an iron atom at the center, surrounded by two cyclopentadienyl rings. One of these cyclopentadienyl rings is substituted with a dimethylaminomethyl group, which is a methyl group bonded to an amino group that itself is bonded to two methyl groups. The molecule also includes a 1,1-diphenylmethanol moiety, which consists of a methanol group (one carbon bonded to a hydroxyl group) with two phenyl rings attached to the carbon. 1-[2-(N,N-dimethylaminomethyl)ferrocenyl]-1,1-diphenylmethanol is known for its potential applications in various fields, including as a ligand in coordination chemistry and in the synthesis of organometallic compounds. Its specific properties and reactivity make it a subject of interest in chemical research and development.

1273-42-3

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1273-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1273-42-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,7 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1273-42:
(6*1)+(5*2)+(4*7)+(3*3)+(2*4)+(1*2)=63
63 % 10 = 3
So 1273-42-3 is a valid CAS Registry Number.

1273-42-3Downstream Products

1273-42-3Relevant academic research and scientific papers

Synthesis of ferrocene derivatives with planar chirality via palladium-catalyzed enantioselective C-H bond activation

Pi, Chao,Cui, Xiuling,Liu, Xiuyan,Guo, Mengxing,Zhang, Hanyu,Wu, Yangjie

supporting information, p. 5164 - 5167 (2014/12/11)

The first catalytic and enantioselective C-H direct acylation of ferrocene derivatives has been developed. A series of 2-acyl-1-dimethylaminomethylferrocenes with planar chirality were provided under highly efficient and concise one-pot conditions with up to 85% yield and 98% ee. The products obtained could be easily converted to various chiral ligands via diverse transformations.

Catalytic and stereoselective ortho-lithiation of a ferrocene derivative

Steffen, Patricia,Unkelbach, Christian,Christmann, Mathias,Hiller, Wolf,Strohmann, Carsten

supporting information, p. 9836 - 9840 (2013/09/23)

N,N-Dimethylferrocenylmethylamine can be lithiated stereoselectively by iPrLi in pentane/Et2O using catalytic amounts of the chiral auxiliary (R,R)-TMCDA. In homogenous reactions, high e.r. values were obtained upon crystallization of the lithiated species. The catalytic activity of TMCDA is made possible by its release from the stereomerically pure lithioferrocene as it dimerizes to a homochiral dimeric etherate. Copyright

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