Capecitabine

  • CasNo:154361-50-9
  • Purity:
  • Molecular Formula:C15H22FN3O6
  • Molecular Weight:359.355
  • Melting Point: 110-121 °C 
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What is the Capecitabine ?

Capecitabine is Colourless solid, while it's Molecular Formula is C15H22FN3O6. An antiproliferative 5-fluorouracil releasing compound

What is the CAS number for Capecitabine ?

The CAS number of Capecitabine is 154361-50-9.

More information of Capecitabine 154361-50-9 are:

Synonyms

Xeloda (TN);Cytidine,5'-deoxy-5-fluoro-N-[(pentyloxy)- carbonyl]-;Pentyl [1-(3,4-dihydroxy-5-methyl-oxolan-2-yl)-5-fluoro-2-oxo-pyrimidin-4-yl]aminoformate;Capecitabine;pentyl (1-((2R,3R,4S,5R)-3,4-dihydroxy-5-methyltetrahydrofuran-2-yl)-5-fluoro-2-oxo-1,2-dihydropyrimidin-4-yl)carbamate;

CAS Number

154361-50-9

Molecular Formula

C15H22FN3O6

Molecular Weight

359.355

Density

1.49 g/cm3

Melting Point

110-121 °C

Boiling Point

437.874oC at 760 mmHg

Flash Point

218.619oC

HS CODE

29349990

PSA

122.91000

LogP

0.83320

Pka

5.41±0.40(Predicted)

What is Capecitabine (154361-50-9) used for?

Capecitabine is a new oral fluoropyrimidine carbamate for patients with advanced neoplastic disease, approved as Xeloda for the treatment of refractory metastatic breast cancer after failure on Paclitaxel and an anthracycline-based chemotherapy regimen ; it is a prodrug of doxifluridine (5-fluorouracil ; 5-FU) activated by a cascade of 3 enzymes concentrated in human liver and cancer tissue, resulting in the selective release of 5-FU at the tumor site and offering a prolonged tumour exposure to 5-FU. Oral Capecitabine passes intact through the intestinal mucosa, is converted first by carboxylesterase to 5'-deoxy-5- fluorocytidine in the liver, then by cytidine deaminase to 5'-deoxy-5-fluorouridine in the liver and tumour tissues and finally by thymidine phosphorylase to 5-FU in tumors. Therefore, Xeloda is much safer and more effective than 5-FU (for example, in the HCT116 human colon cancer and the MX-1 breast cancer xenograft .models).

InChI:InChI=1/C9H12FN3O4/c1-3-5(14)6(15)8(17-3)13-2-4(10)7(11)12-9(13)16/h2-3,5-6,8,14-15H,1H3,(H2,11,12,16)/t3-,5-,6-,8-/m1/s1

Articles related to Capecitabine:

Article

Source

Synthesis of the antitumoral nucleoside capecitabine through a chemo-enzymatic approach

Ciceri, Samuele,Ciuffreda, Pierangela,Grisenti, Paride,Ferraboschi, Patrizia

, p. 5909 - 5913 (2015)

Preparation of capecitabine intermediate

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Paragraph 0025-0028, (2021/09/01)

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