
Capecitabine Powder
CAS:154361-50-9
Specification : 99%
Appearance: White powder
Shelf life:2 years
Advantage:
Sample is Available
High purity, Top quality and best price
COA, HPLC, MSDS available
Certificate: ISO,GMP,CTC,SGS,CQC
Place of Origin: Shandong, China
Description
Pharmaceutical Raw Material CAS 154361-50-9 99% Purity Capecitabine
| Product Name | Capecitabine | Customized | Customized |
| CAS | 154361-50-9 | MF | C15H22FN3O6 |
| Specification | 99% HPLC | MW | 359.35 |
|
Appearance |
White Powder | EINECS | 604-948-1 |
| Storage | Cool Dry Place | ||
|
Shelf Life |
2 years |
||
|
Grade |
Pharmaceutical Grade | Origin | Shandong China |
What Is Capecitabine Powder?
Capecitabine serves as a primary treatment option for patients diagnosed with colorectal cancer. Additionally, it is administered either alone or in conjunction with docetaxel to individuals with metastatic breast cancer who have undergone anthracycline therapy but have experienced disease advancement or recurrence.
Besides causing bone marrow suppression, nausea, and vomiting, this medication can also lead to severe diarrhea and a potentially debilitating condition known as "hand-and-foot syndrome" (palmar-plantar erythrodysesthesia). By inhibiting CYP2C9 and competing for serum protein binding sites, capecitabine can produce clinically relevant drug interactions with both warfarin and phenytoin.
Capecitabine (capecitabine) is an antimetabolizing fluoropyrimidine deoxyriboside carbamate that can be converted to 5-FU in vivo by a synthetic route:
Starting with D-ribose, after methylation of the 1-hydroxy group and protection of the 2,3-hydroxy groups, 2,3-O-isopropylidene-D-furanosyl methyl glycoside is obtained.
Reacting with p-toluenesulfonyl chloride in the presence of pyridine yields 2,3-O-isopropylidene-5-O-p-toluenesulfonyl-D-furanosyl methyl glycoside.
Subsequent iodination with sodium iodide gives 2,3-O-isopropylidene-5-iodo-D-furanosyl methyl glycoside.
Reduction with Pd/C catalytic hydrogenation results in 2,3-O-isopropylidene-5-deoxy-D-furanosyl methyl glycoside.
Deprotection with sulfuric acid and acetylation with acetic anhydride yield 1,2,3-tri-O-acetyl-5-deoxy-D-ribose.
Condensation with 5-fluorouracil in the presence of anhydrous tin tetrachloride produces 2',3'-di-O-acetyl-5'-deoxy-5-fluorocytidine.
Reaction of 2',3'-di-O-acetyl-5'-deoxy-5-fluorocytidine with pentyl chloroformate gives 2',3'-di-O-acetyl-5'-deoxy-5-fluoro-N4-[(pentyloxy)carbonyl]cytidine.
Finally, hydrolysis with sodium hydroxide yields the final product, Capecitabine.


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