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148278-96-0

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148278-96-0 Usage

General Description

(R)-2-AMINO-3-METHOXY-1-PROPANOL is a chemical compound with the molecular formula C4H11NO2. It is a chiral compound, meaning it has a non-superimposable mirror image, and the prefix "(R)" indicates the absolute configuration of its stereochemistry. (R)-2-AMINO-3-METHOXY-1-PROPANOL is commonly used as a chiral building block in the synthesis of pharmaceuticals and agrochemicals. It also has potential applications in the production of chiral catalysts and ligands. (R)-2-AMINO-3-METHOXY-1-PROPANOL is known to have a role in the synthesis of various drugs, including the anti-cancer drug bosutinib, and the chiral cross-coupling reagent Pd-dba-L. Moreover, it possesses unique physicochemical properties such as being a good solvent for the resolution of racemic mixtures. Overall, this compound is widely utilized in the chemical and pharmaceutical industries due to its chiral nature and unique functional groups.

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

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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.

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