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(S)-Ftorafur is a chemotherapeutic drug that serves as an oral prodrug of 5-fluorouracil (5-FU), a potent anti-cancer agent. It is designed to treat various types of cancer by converting into 5-FU within the body, where it disrupts the synthesis of DNA and RNA, leading to cancer cell death. Known for its effectiveness when combined with other chemotherapy agents, (S)-Ftorafur is a well-tolerated drug that is often included in standard chemotherapy regimens.

55774-30-6

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55774-30-6 Usage

Uses

Used in Oncology:
(S)-Ftorafur is used as a chemotherapeutic agent for the treatment of various cancers, such as colorectal, breast, and stomach cancer. It functions by converting into 5-FU in the body, which interferes with the synthesis of DNA and RNA, ultimately causing cell death in cancerous tissues.
Used in Combination Chemotherapy:
(S)-Ftorafur is used as a component in combination chemotherapy to enhance the effectiveness of cancer treatment. Its synergistic action with other chemotherapy agents helps maximize the killing of cancer cells and improve patient outcomes.
Used in Pharmaceutical Development:
(S)-Ftorafur serves as a model for the development of new oral prodrugs with improved pharmacokinetics, bioavailability, and reduced side effects, potentially leading to the creation of more effective and safer cancer treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 55774-30-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,7 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55774-30:
(7*5)+(6*5)+(5*7)+(4*7)+(3*4)+(2*3)+(1*0)=146
146 % 10 = 6
So 55774-30-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H9FN2O3/c9-5-4-11(6-2-1-3-14-6)8(13)10-7(5)12/h4,6H,1-3H2,(H,10,12,13)/t6-/m0/s1

55774-30-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-tetrahydrofuryl)-5-fluorouracil

1.2 Other means of identification

Product number -
Other names (S)-1-(Tetrahydrofuran-2-yl)-5-fluorouracil

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:55774-30-6 SDS

55774-30-6Upstream product

55774-30-6Downstream Products

55774-30-6Relevant academic research and scientific papers

Pd-Catalyzed Regioselective Asymmetric Addition Reaction of Unprotected Pyrimidines to Alkoxyallene

Kang, Soyeong,Jang, Seok Hyeon,Lee, Juyeol,Kim, Dong-Gil,Kim, Mijin,Jeong, Wook,Rhee, Young Ho

, p. 4684 - 4687 (2017)

Catalytic asymmetric synthesis of N-heterocyclic glycosides free of protecting and directing groups is reported. The key reaction is highlighted by the atom-efficient and regioselective addition of unprotected pyrimidines to highly functionalized alkoxyal

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