CAS 123982-81-0

(S)-3-(1-AMINO-ETHYL)-PHENOL

Description:

(S)-3-(1-Amino-ethyl)-phenol, also known as (S)-3-(2-aminoethyl)phenol, is an organic compound characterized by the presence of a phenolic hydroxyl group and an aminoethyl side chain. This compound is a chiral molecule, with the (S) configuration indicating the specific spatial arrangement of its atoms. It typically appears as a solid or crystalline substance and is soluble in polar solvents due to the presence of both the hydroxyl and amino groups, which can engage in hydrogen bonding. The amino group imparts basic properties, allowing it to participate in various chemical reactions, including those typical of amines. This compound may be of interest in pharmaceutical research and development, particularly in the synthesis of biologically active molecules or as a potential intermediate in drug formulation. Its properties, such as melting point, boiling point, and reactivity, can vary based on environmental conditions and the presence of other functional groups in a reaction mixture. Safety data should be consulted for handling and storage, as with any chemical substance.

Formula: C₈H₁₁NO

InChI: InChI=1/C8H11NO/c1-6(9)7-3-2-4-8(10)5-7/h2-6,10H,9H2,1H3/t6-/m0/s1

SMILES: C[C@@H](c1cccc(c1)O)N

Synonyms:

• 3-[(1S)-1-Aminoethyl]Phenol
• Phenol, 3-[(1S)-1-aminoethyl]-

Phenol, 3-[(1S)-1-aminoethyl]-

CAS: 123982-81-0

Formula: C₈H₁₁NO

Purity: 97%

Color and Shape: Solid

Molecular weight: 137.1790

Ref: IN-DA000LBE

(S)-3-(1-Aminoethyl)phenol

CAS: 123982-81-0

(S)-3-(1-Aminoethyl)phenol

Purity: 95%

Molecular weight: 137.18g/mol

Ref: 54-OR1006540

Rivastigmine Impurity 15

CAS: 123982-81-0

Formula: C₈H₁₁NO

Molecular weight: 137.18

Ref: 4Z-R-0739

(S)-3-(1-Aminoethyl)phenol

CAS: 123982-81-0

Purity: 95%

Color and Shape: Liquid

Molecular weight: 137.1820068

Ref: 10-F787705

(S)-3-(1-Aminoethylphenol

CAS: 123982-81-0

(S)-3-(1-Aminoethylphenol) is a polypeptide that has significant activity in neuropathic pain and diabetic neuropathy. It is an enantiomer of the racemic mixture of (R)-3-(1-Aminoethylphenol). It is synthesized by biocatalysts from 2-chloroethanol in the presence of acrylamide and formaldehyde. The discovery of this compound was made possible by screening for compounds that could inhibit the enzyme transaminase, which plays a role in the metabolism of L-DOPA to dopamine. This compound binds to host cells and blocks the synthesis of polypeptides, which may be involved in the pathogenesis of neuropathic pain.

Purity: Min. 95%

Ref: 3D-FA57616