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110826-96-5

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110826-96-5 Usage

General Description

2-amino-1-(4-phenylphenyl)ethan-1-ol, also known as 4-phenylphenethylamine, is a chemical compound with the molecular formula C16H17NO. It is categorized as an organic compound and belongs to the family of phenethylamines. 2-amino-1-(4-phenylphenyl)ethan-1-ol consists of a phenethylamine core with a phenyl group attached to the amino group and a hydroxyl group at the alpha carbon, resulting in a chiral center. 4-phenylphenethylamine is commonly used in the synthesis of various pharmaceuticals and research chemicals. It exhibits psychoactive properties and is known for its stimulatory effects on the central nervous system. Additionally, 4-phenylphenethylamine is utilized in the development of new drugs for treating various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 110826-96-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,8,2 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110826-96:
(8*1)+(7*1)+(6*0)+(5*8)+(4*2)+(3*6)+(2*9)+(1*6)=105
105 % 10 = 5
So 110826-96-5 is a valid CAS Registry Number.

110826-96-5Downstream Products

110826-96-5Relevant articles and documents

Easy kinetic resolution of some β-amino alcohols by Candida antarctica lipase B catalyzed hydrolysis in organic media

Alalla, Affef,Merabet-Khelassi, Mounia,Riant, Olivier,Aribi-Zouioueche, Louisa

supporting information, p. 1253 - 1259 (2016/11/23)

Herein, we present an easy and eco-friendly pathway to obtain some enantiomerically enriched β-amino alcohols using essentially as β-blockers. The enzymatic hydrolysis is conducted in hydrophobic organic media, assisted by sodium carbonate and CAL-B. We describe a new and effective procedure in terms of the chemo- and enantioselectivity, which allows for the formation of both enantiomers: the 2-acetamido-1-arylacetates and 2-acetamido-1-arylethanols were obtained with high ee values (up to >99%), while the selectivities reached E >200. The obtained results show a high CAL-B affinity toward the deacylation of the 2-acetamido-1-arylacetates compared to the acylation one. The structure of the 2-acetamido-1-arylacetates had a significant influence on both reactivity and selectivity of the CAL-B catalyzed deacylation. A multigram scale O-deacylation of racemic 2-acetamido-1-phenylacetate has been carried out, giving access both enantiomers with high enantiomeric purity and good isolated chemical yields.

ARYL-HYDROXYETHYLAMINO-PYRIMIDINES AND TRIAZINES AS MODULATORS OF FATTY ACID AMIDE HYDROLASE

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Page/Page column 124, (2009/10/18)

Certain aryl-hydroxyethylamino-pyrimidine and triazine compounds are described, which are useful as FAAH inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by fatty acid amide hydrolase (FAAH) activity, such as anxiety, pain, inflammation, sleep disorders, eating disorders, energy metabolism disorders, and movement disorders (e.g., multiple sclerosis). Methods of synthesizing such compounds are also disclosed.

Directional probes of the hydrophobic component of the aromatic ring binding site of norepinephrine N-methyltransferase

Rafferty,Borchardt,Grunewald

, p. 1204 - 1208 (2007/10/02)

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