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1985607-83-7

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1985607-83-7 Usage

General Description

Zofluza intermediate refers to an intermediate substance used in the preparation of Zofluza, a prescription medicine used to treat influenza in individuals above the age of 12. Zofluza (otherwise known as Baloxavir Marboxil) works by inhibiting the replication of the influenza virus within the body, thereby easing symptoms and reducing the duration of the illness. The exact chemical structure or process involving the Zofluza intermediate isn't publicly disclosed due to the proprietary nature of pharmaceutical manufacturing. Like many pharmaceutical intermediates, they are valuable for fine-tuning chemical reactions to produce the final active pharmaceutical ingredient (API).

Check Digit Verification of cas no

The CAS Registry Mumber 1985607-83-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,9,8,5,6,0 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1985607-83:
(9*1)+(8*9)+(7*8)+(6*5)+(5*6)+(4*0)+(3*7)+(2*8)+(1*3)=237
237 % 10 = 7
So 1985607-83-7 is a valid CAS Registry Number.

1985607-83-7Relevant articles and documents

Pyridazone derivative and its uses

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Paragraph 0163, (2022/01/12)

The present invention belongs to the pharmaceutical field, specifically relates to a pyridazone derivative and its uses, compounds thereof and pharmaceutically acceptable salts, solvates including hydrates, polycrystallines, prodrugs, co-crystallines, tau

Preparation method of sulfur-containing hetero-seven-membered ring compound

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Paragraph 0043-0044; 0065-0068, (2021/06/13)

The invention relates to a preparation method of a sulfur-containing hetero-seven-membered ring compound. The method comprises the following steps: carrying out halogenation reaction, nucleophilic substitution, acylation, cyclization, reduction and the li

Synthesis method of baloxavir marboxil intermediate

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Paragraph 0029-0033, (2021/05/19)

The invention discloses a synthesis method of a baloxavir marboxil intermediate. The synthesis method comprises the following steps of: taking 7,8-difluorodibenzo[B,E]thiophene-11(6H)-ketone as a raw material, adopting chloro(R,R)-N-(tosyl)-1,2-diphenyl ethylene diamine(chloro)(p-propyl toluene) ruthenium (II) or chloro(S,S)-N-(tosyl)-1,2-diphenyl ethylene diamine(chloro)(p-propyl toluene) ruthenium (II) as a catalyst, reducing carbonyl into chiral alcohol so as to obtain an intermediate namely chiral 7,8-difluoro-dihydrodibenzo[b,e]thiepin-11-ol for synthesizing baloxavir marboxil. The optical purity of baloxavir marboxil synthesized from the intermediate is 98.0% or more, the subsequent purification processes are reduced, the yield is increased, the cost is reduced, and the synthesis method is more suitable for commercial production.

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