291545-74-9 Usage
Description
(S)-2-chloro-N-(2-hydroxyl-1-phenylethyl)acetamide is a chemical compound with the molecular formula C10H12ClNO2. It is a derivative of acetamide, containing a chlorine atom and a hydroxyl group attached to a phenylethyl moiety. (S)-2-chloro-N-(2-hydroxyl-1-phenylethyl)acetamide is a potential chiral building block that can be utilized in the synthesis of pharmaceuticals and other biologically active molecules. Its structural features and potential biological activities make it a promising candidate for applications in medicinal chemistry and drug discovery. The stereochemistry of the compound may also play a critical role in determining its pharmacological properties and interactions with biological targets.
Uses
Used in Pharmaceutical Synthesis:
(S)-2-chloro-N-(2-hydroxyl-1-phenylethyl)acetamide is used as a chiral building block for the synthesis of pharmaceuticals and biologically active molecules. Its unique structural features and potential biological activities contribute to the development of new drugs and therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-2-chloro-N-(2-hydroxyl-1-phenylethyl)acetamide is used as a valuable chemical intermediate. Its stereochemistry and potential interactions with biological targets make it a promising candidate for the development of bioactive compounds and pharmaceutical products.
Used in Drug Discovery:
(S)-2-chloro-N-(2-hydroxyl-1-phenylethyl)acetamide is also used in drug discovery due to its potential to be a key component in the creation of new drugs. Its structural features and potential biological activities can be harnessed to identify and develop novel therapeutic agents for various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 291545-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,1,5,4 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 291545-74:
(8*2)+(7*9)+(6*1)+(5*5)+(4*4)+(3*5)+(2*7)+(1*4)=159
159 % 10 = 9
So 291545-74-9 is a valid CAS Registry Number.
291545-74-9Relevant articles and documents
SUBSTITUTED MORPHOLINE DERIVATIVES AS ROR GAMMA MODULATORS
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Page/Page column 23, (2018/07/29)
The present disclosure is directed to compounds of formula (I) and pharmaceutically acceptable salts thereof, wherein ring A, R1, R2, R3, X1, X2, m and n are as defined herein, which are active as modulators of retinoid-related orphan receptor gamma t (RORyt). These compounds prevent, inhibit, or suppress the action of RORyt and are therefore useful in the treatment of RORyt mediated diseases, disorders, syndromes or conditions such as, e.g., pain, inflammation, COPD, asthma, rheumatoid arthritis, colitis, multiple sclerosis, psoriasis, neurodegenerative diseases and cancer. (I)
TRICYCLIC MODULATORS OF TNF SIGNALING
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Page/Page column 144, (2016/11/02)
The invention provides tricyclic heterocyclic compounds, pharmaceutically acceptable salts, prodrugs, biologically active metabolites, stereoisomers and isomers thereof wherein the variables are defined herein. The compounds of the invention may be useful for treating immunological and oncological conditions.
Amine-promoted asymmetric (4+2) annulations for the enantioselective synthesis of tetrahydropyridines: A traceless and recoverable auxiliary strategy
Hu, Pengfei,Hu, Jian,Jiao, Jiajun,Tong, Xiaofeng
supporting information, p. 5319 - 5322 (2013/06/05)
Gone, without a trace: The in situ reaction of 2-(acetoxymethyl)buta-2,3- dienoate and a secondary amine produces a 2-methylene-3-oxobutanoate equivalent that can be used in asymmetric [4+2] annulations with N-tosylimines to provide tetrahydropyridines in
