27948-38-5 Usage
Description
(1S)-Methyl-2-furanylMethylaMine, a chemical compound with the molecular formula C7H9NO, is a derivative of furfural, a natural organic compound found in a variety of plants. It has potential pharmaceutical applications and is used in the synthesis of various drugs and biologically active molecules. (1S)-Methyl-2-furanylMethylaMine has been studied for its potential neuroprotective and anti-inflammatory properties, and may have potential applications in the treatment of neurological and inflammatory diseases. Additionally, (1S)-Methyl-2-furanylMethylaMine has been investigated for its potential role in cancer therapy, as it may have anti-tumor and cytotoxic effects. Overall, this compound has potential applications in the fields of pharmaceuticals, medicine, and biotechnology.
Uses
Used in Pharmaceutical Industry:
(1S)-Methyl-2-furanylMethylaMine is used as a building block for the synthesis of various drugs and biologically active molecules, contributing to the development of new therapeutic agents.
Used in Medicine:
(1S)-Methyl-2-furanylMethylaMine is used as a potential neuroprotective and anti-inflammatory agent, with potential applications in the treatment of neurological and inflammatory diseases.
Used in Biotechnology:
(1S)-Methyl-2-furanylMethylaMine is used as a potential candidate for cancer therapy, with potential anti-tumor and cytotoxic effects, offering new avenues for the development of cancer treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 27948-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,4 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 27948-38:
(7*2)+(6*7)+(5*9)+(4*4)+(3*8)+(2*3)+(1*8)=155
155 % 10 = 5
So 27948-38-5 is a valid CAS Registry Number.
27948-38-5Relevant articles and documents
Asymmetric Synthesis of Chiral Primary Amines by Ruthenium-Catalyzed Direct Reductive Amination of Alkyl Aryl Ketones with Ammonium Salts and Molecular H2
Tan, Xuefeng,Gao, Shuang,Zeng, Weijun,Xin, Shan,Yin, Qin,Zhang, Xumu
supporting information, p. 2024 - 2027 (2018/02/19)
A ruthenium/C3-TunePhos catalytic system has been identified for highly efficient direct reductive amination of simple ketones. The strategy makes use of ammonium acetate as the amine source and H2 as the reductant and is a user-friendly and operatively simple access to industrially relevant primary amines. Excellent enantiocontrol (>90% ee for most cases) was achieved with a wide range of alkyl aryl ketones. The practicability of this methodology has been highlighted by scalable synthesis of key intermediates of three drug molecules. Moreover, an improved synthetic route to the optimal diphosphine ligand C3-TunePhos is also presented.
Candida antarctica lipase-catalyzed doubly enantioselective aminolysis reactions. Chemoenzymatic synthesis of 3-hydroxypyrrolidines and 4-(silyloxy)-2-oxopyrrolidines with two stereogenic centers
Sanchez, Victor M.,Rebolledo, Francisca,Gotor, Vicente
, p. 1464 - 1470 (2007/10/03)
Aminolyses of racemic and prochiral 3-hydroxyesters with racemic amines are effectively catalyzed by Candida antarctica lipase. In these processes, the simultaneous resolution of the ester and the amine, or the corresponding asymmetrization-resolution, takes place. In all cases, the high enantioselectivity shown by the lipase toward all the reactants allows the preparation of enantiopure 3-hydroxyamides with very high diastereomeric ratios. These 3-hydroxyamides are used as starting materials in the synthesis of 3-hydroxy-and 2-oxopyrrolidines, both containing two stereogenic centers in their structures.
