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1-(4-fluorophenyl)butan-1-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

321839-98-9

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321839-98-9 Usage

Type of compound

Amine

Nitrogen atom

Bonded to at least one hydrogen atom

Structure

Contains a butyl chain (4-carbon) with a fluorine-substituted phenyl ring at one end

Usage

Organic synthesis and pharmaceutical research

Potential applications

Development of new drugs and pharmaceutical products

Field of interest

Neuroscience and central nervous system research

Biological and pharmacological properties

Not well-documented

Chemical structure

Allows for potential functionalization and modification to create new compounds with specific desired properties and applications

Check Digit Verification of cas no

The CAS Registry Mumber 321839-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,8,3 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 321839-98:
(8*3)+(7*2)+(6*1)+(5*8)+(4*3)+(3*9)+(2*9)+(1*8)=149
149 % 10 = 9
So 321839-98-9 is a valid CAS Registry Number.

321839-98-9Relevant academic research and scientific papers

METALLOENZYME INHIBITOR COMPOUNDS

-

, (2018/09/28)

Provided are compounds having HDAC6 modulating activity, and methods of treating diseases, disorders or symptoms thereof mediated by HDAC6.

Synthesis of enantiopure 1-aryl-1-butylamines and 1-aryl-3-butenylamines by diastereoselective addition of allylzinc bromide to imines derived from (R)-phenylglycine amide

Dalmolen, Jan,Van Der Sluis, Marcel,Nieuwenhuijzen, Jose W.,Meetsma, Auke,De Lange, Ben,Kaptein, Bernard,Kellogg, Richard M.,Broxterman, Quirinus B.

, p. 1544 - 1557 (2007/10/03)

The synthesis of enantiopure 1-aryl-1-butylamines via a highly diastereoselective addition of allylzinc bromide to imines derived from (R)-phenylglycine amide is reported. These are synthesised by a three-step procedure, which involves: (a) formation of the chiral imines; (b) asymmetric addition of the allylzinc reagent; (c) removal of the chiral auxiliary by means of a reductive or non-reductive method. The reductive method provides 1-aryl-1-butylamines whereas the non-reductive method preserves the double bond to afford 1-aryl-3-butenylamines. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

Synthesis of optically-active benzylic amines; asymmetric reduction of ketoxime ethers with chiral oxazaborolidines

Fontaine, Evelyne,Namane, Claudie,Meneyrol, Jerome,Geslin, Michel,Serva, Laurence,Roussey, Eliane,Tissandie, Stephanie,Maftouh, Mohamed,Roger, Pierre

, p. 2185 - 2189 (2007/10/03)

The preparation of novel optically active benzylic amines by the enantioselective reduction of phenone oximes using chiral oxazaborolidine is described. The choice of the chiral 1,2-amino alcohol (S)-diphenylvalinol as chiral inducer and that of the benzy

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