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Benzyl-(2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-amine is a complex organic compound with the molecular formula C15H17NO2. It is characterized by a benzylamine group attached to a 2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl moiety. BENZYL-(2,3-DIHYDRO-BENZO[1,4]DIOXIN-2-YLMETHYL)-AMINE is part of a class of chemicals known as benzylamines, which are derivatives of benzylamine with various substituents. The specific structure of BENZYL-(2,3-DIHYDRO-BENZO[1,4]DIOXIN-2-YLMETHYL)-AMINE involves a benzene ring fused to a dioxin ring, with a nitrogen atom in the side chain. It is likely to be used in chemical research or as an intermediate in the synthesis of more complex molecules, given its unique structure and potential reactivity. However, without specific context or application, it's challenging to provide a more detailed summary of its uses or properties.

2164-42-3

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2164-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2164-42-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2164-42:
(6*2)+(5*1)+(4*6)+(3*4)+(2*4)+(1*2)=63
63 % 10 = 3
So 2164-42-3 is a valid CAS Registry Number.

2164-42-3Downstream Products

2164-42-3Relevant academic research and scientific papers

Nickel-Catalyzed Reduction of Secondary and Tertiary Amides

Simmons, Bryan J.,Hoffmann, Marie,Hwang, Jaeyeon,Jackl, Moritz K.,Garg, Neil K.

supporting information, p. 1910 - 1913 (2017/04/11)

The nickel-catalyzed reduction of secondary and tertiary amides to give amine products is reported. The transformation is tolerant of extensive variation with respect to the amide substrate, proceeds in the presence of esters and epimerizable stereocenters, and can be used to achieve the reduction of lactams. Moreover, this methodology provides a simple tactic for accessing medicinally relevant α-deuterated amines.

Some potential α-adrenoreceptor blocking 1,4-benzodioxanes and 2,6-dimethoxyphenoxyethylamines

Dewar,Kapur,Mottram

, p. 286 - 290 (2007/10/02)

The synthesis and α-adrenoreceptor blocking activity of a series of 1,4-benzodioxanes and 2,6-dimethoxyphenoxyethylamines has been described. A number of analogues exhibited α-blockade, but none approached the potency of the benzodioxane WB 4101. Some mem

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