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1628206-34-7

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1628206-34-7 Usage

General Description

Phenyl (6-methylpyridin-3-yl)carbamate hydrochloride is a chemical compound used as an intermediate in the production of pharmaceuticals and agricultural chemicals. It is a carbamate derivative with a phenyl group attached to the nitrogen atom of a pyridine ring. The hydrochloride salt form of this compound enhances its solubility in water, making it more suitable for certain applications. This chemical may exhibit insecticidal or fungicidal properties due to its carbamate structure, and can also be used as a reagent in organic synthesis reactions. Proper handling and storage of phenyl (6-methylpyridin-3-yl)carbamate hydrochloride is important to ensure its stability and prevent potential hazards associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 1628206-34-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,8,2,0 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1628206-34:
(9*1)+(8*6)+(7*2)+(6*8)+(5*2)+(4*0)+(3*6)+(2*3)+(1*4)=157
157 % 10 = 7
So 1628206-34-7 is a valid CAS Registry Number.

1628206-34-7Relevant articles and documents

Development of a Factory Process for Omecamtiv Mecarbil, a Novel Cardiac Myosin Activator

Caille, Seb,Allgeier, Alan M.,Bernard, Charles,Correll, Tiffany L.,Cosbie, Andrew,Crockett, Richard D.,Cui, Sheng,Faul, Margaret M.,Hansen, Karl B.,Huggins, Seth,Langille, Neil,Mennen, Steven M.,Morgan, Bradley P.,Morrison, Henry,Muci, Alexander,Nagapudi, Karthik,Quasdorf, Kyle,Ranganathan, Krishnakumar,Roosen, Philipp,Shi, Xianqing,Thiel, Oliver R.,Wang, Fang,Tvetan, Justin T.,Woo, Jacqueline C. S.,Wu, Steven,Walker, Shawn D.

, p. 1558 - 1567 (2019/09/04)

The development of a factory process to manufacture the novel cardiac myosin activator omecamtiv mecarbil (1) is described. Omecamtiv mecarbil is prepared via the convergent synthesis and coupling of two key fragments, aniline 2 and carbamate 4-HCl, which serves as a masked isocyanate. To enable practical access to aniline 2, reduction of the corresponding nitroaromatic was designed to control potential mutagenic impurities. Key to the efficient preparation of 2 was the benzylic bromination of 8 followed by selective debromination of a gem-dibromide byproduct and subsequent alkylation with 5-phosphate. Overall, the longest linear sequence consists of six steps, including a final salt formation step to afford the drug substance in 55% overall yield. Because of poor performance of the original free-base form of the drug substance in modified-release formulations, an improved dihydrochloride hydrate form was developed to aid drug product performance and manufacturability.

HETEROCYCLIC COMPOUNDS AND THEIR USES

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Paragraph 0093-0094, (2014/10/04)

Provided are certain pharmaceutical formulations of omecamtiv mecarbil and methods for their preparation and use.

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