Cas:924871-61-4 3-Bromo-8-(phenylsulfonyl)-1-oxa-8-azaspiro[4.5]decane manufacturer & supplier

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3-Bromo-8-(phenylsulfonyl)-1-oxa-8-azaspiro[4.5]decane

Chemical Name:3-Bromo-8-(phenylsulfonyl)-1-oxa-8-azaspiro[4.5]decane
CAS.NO:924871-61-4
Synonyms:3-Bromo-8-(phenylsulfonyl)-1-oxa-8-azaspiro[4.5]decane
Molecular Formula:C14H18BrNO3S
Molecular Weight:360.26700
HS Code:

Physical and Chemical Properties:
Melting point:N/A
Boiling point:485.783ºC at 760 mmHg
Density:1.563g/cm3
Index of Refraction:1.629
PSA:54.99000
Exact Mass:359.01900
LogP:3.41240

Material Safety Information (Applicable for Hazard Chemicals)
RIDADR:
Packing Group:


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Related News: After this long manufacturing process, it is purified until it reaches a very high degree of purity and finally becomes an API. 3-Bromo-8-(phenylsulfonyl)-1-oxa-8-azaspiro[4.5]decane manufacturer In addition, the FDA approval ignored the recommendation of its outside advisors, who said Biogen did not provide enough evidence of clinical benefit. Three of the advisory panel’s members have resigned in protest since the FDA decision was announced on Monday. 3-Bromo-8-(phenylsulfonyl)-1-oxa-8-azaspiro[4.5]decane supplier In addition, the FDA approval ignored the recommendation of its outside advisors, who said Biogen did not provide enough evidence of clinical benefit. Three of the advisory panel’s members have resigned in protest since the FDA decision was announced on Monday. 3-Bromo-8-(phenylsulfonyl)-1-oxa-8-azaspiro[4.5]decane vendor At present, Teva can produce more than 300 generic drugs, and the API department has approximately 650 authorized patents and patent applications worldwide. It is also the generic drug company with the most challenges in patenting ParagraphIV in the world. 3-Bromo-8-(phenylsulfonyl)-1-oxa-8-azaspiro[4.5]decane factory In recent years, China’s bulk drug companies have gradually completed the upgrade of the product structure of bulk raw materials to specialty raw materials and intermediates. The industry’s leading companies have further developed the research and development layout of high-barrier generic pharmaceutical raw materials with multiple patents that have not yet expired.