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Butanoic acid, 4-[[(2-hydroxyphenyl)methyl]amino]-, also known as 4-[(2-hydroxybenzyl)amino]butanoic acid, is an organic compound with the chemical formula C11H15NO3. It is a derivative of butanoic acid, featuring a 2-hydroxyphenylmethylamine group attached to the 4-position of the butanoic acid backbone. Butanoic acid, 4-[[(2-hydroxyphenyl)methyl]amino]- is characterized by its molecular weight of 205.24 g/mol and a melting point of approximately 90-92°C. It is a white crystalline solid and is soluble in water and various organic solvents. This chemical is primarily used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of certain drugs and active ingredients. Its unique structure, combining a carboxylic acid group with an aromatic amine, endows it with specific chemical properties that make it valuable in the development of new medications.

2171-71-3

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2171-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2171-71-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,7 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2171-71:
(6*2)+(5*1)+(4*7)+(3*1)+(2*7)+(1*1)=63
63 % 10 = 3
So 2171-71-3 is a valid CAS Registry Number.

2171-71-3Downstream Products

2171-71-3Relevant academic research and scientific papers

New Biologically Active Aromatic Derivatives of Fatty Acids

Lurie, E. Yu.,Kaplun, A. P.,Kulakov, V. N.,Shvets, V. I.

, p. 264 - 268 (2007/10/02)

A convenient method for synthesizing the homologous series of new aromatic derivatives of fatty acids is described.The synthetic approach includes the reductive alkylation of ω- and α-amino acids with hydroxybenzaldehydes.The physicochemical properties of

Transition-state analogues as inhibitors for GABA-aminotransferase

Iskander, MN,Andrews, PR,Winkler, DA,Brinkworth, RI,Paola, C Di,et al.

, p. 129 - 136 (2007/10/02)

Our previous calculations on the reaction catalysed by GABA-aminotransferase (GABA-T) have been utilized in this work in order to synthesize a series of reversible inhibitors of this enzyme.The synthesized transition-state analogues and their precursors i

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