148278-96-0 Usage
Description
(R)-2-AMINO-3-METHOXY-1-PROPANOL, with the molecular formula C4H11NO2, is a chiral compound that features a non-superimposable mirror image. The prefix "(R)" denotes the specific absolute configuration of its stereochemistry. (R)-2-AMINO-3-METHOXY-1-PROPANOL is recognized for its significance in the chemical and pharmaceutical industries, primarily as a chiral building block in the synthesis of pharmaceuticals and agrochemicals. It also holds potential in the creation of chiral catalysts and ligands, and is utilized in the production of specific drugs and as a solvent for resolving racemic mixtures.
Uses
Used in Pharmaceutical Synthesis:
(R)-2-AMINO-3-METHOXY-1-PROPANOL is used as a chiral building block for the development of various pharmaceuticals, leveraging its unique stereochemistry to create enantiomerically pure compounds, which is crucial for the efficacy and safety of many drugs.
Used in Agrochemical Production:
In the agrochemical industry, (R)-2-AMINO-3-METHOXY-1-PROPANOL serves as a key component in the synthesis of biologically active compounds, contributing to its effectiveness and selectivity in agricultural applications.
Used in the Synthesis of Chiral Catalysts and Ligands:
(R)-2-AMINO-3-METHOXY-1-PROPANOL is utilized as a precursor in the production of chiral catalysts and ligands, which are essential in asymmetric synthesis and other chemical reactions requiring stereoselectivity.
Used in the Synthesis of Specific Drugs:
(R)-2-AMINO-3-METHOXY-1-PROPANOL plays a role in the synthesis of drugs like the anti-cancer medication bosutinib, highlighting its importance in the development of life-saving pharmaceuticals.
Used as a Solvent for Racemic Mixture Resolution:
(R)-2-AMINO-3-METHOXY-1-PROPANOL is known for its good solvent properties, making it suitable for the resolution of racemic mixtures, which is vital for obtaining pure enantiomers in the pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 148278-96-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,2,7 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 148278-96:
(8*1)+(7*4)+(6*8)+(5*2)+(4*7)+(3*8)+(2*9)+(1*6)=170
170 % 10 = 0
So 148278-96-0 is a valid CAS Registry Number.
148278-96-0Relevant articles and documents
PYRIDAZINONES AS PARP7 INHIBITORS
-
Paragraph 1709, (2019/11/11)
The present invention relates to pyridazinones and related compounds which are inhibitors of PARP7 and are useful in the treatment of cancer.
Concise synthesis of (+)-serinolamide A
Gao, Ya-Ru,Guo, Shi-Huan,Zhang, Zhuan-Xiang,Mao, Shuai,Zhang, Yan-Lei,Wang, Yong-Qiang
, p. 6511 - 6513 (2013/11/19)
Serinolamide A, isolated from a species of marine cyanobacteria, exhibits a moderate agonist effect and selectivity for the CB1 cannabinoid receptor, which is unusual for marine natural products. Herein, we reported a highly efficient enantiospecific first total synthesis of (+)-serinolamide A from l-serine in nine steps with 30% overall yield. The synthesis method provides a facile, practicable, and economical approach for the preparation of other similar endocanabinoid lipids.
