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1-Butyl-5-fluorouracil is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69243-15-8

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69243-15-8 Usage

Derived from

5-fluorouracil (5-FU)

Type of compound

chemical compound

Use

cancer treatment (prodrug)

Active form

5-FU (converted in the body)

Designed to be

more effective and less toxic than 5-FU

Potential treatment for

colorectal and breast cancer

Mechanism of action

inhibiting the growth of cancer cells by interfering with their ability to replicate and repair DNA

Ongoing research goal

improving cancer treatment outcomes and minimizing side effects for patients

Check Digit Verification of cas no

The CAS Registry Mumber 69243-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,4 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69243-15:
(7*6)+(6*9)+(5*2)+(4*4)+(3*3)+(2*1)+(1*5)=138
138 % 10 = 8
So 69243-15-8 is a valid CAS Registry Number.

69243-15-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-butyl-5-fluoropyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 1-Butan-1-sulfonyl-5-fluor-1H-pyrimidin-2,4-dion

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:69243-15-8 SDS

69243-15-8Downstream Products

69243-15-8Relevant academic research and scientific papers

Application of the Benzyloxycarbonyloxymethyl Moiety to a Protective Group of 5-Fluoroacil. Selective Alkylation of Amide Nitrogen of the Uracil Ring

Nagase, Toshio,Seike, Kanzo,Shiraishi, Kazuto,Yamada, Yutaka,Ozaki, Shoichiro

, p. 1381 - 1384 (2007/10/02)

Selective alkylation of 5-fluorouracil using the benzoyloxycarbonyloxymethyl moiety as a protective group of amide nitrogen of the uracil ring is described.Protection, alkylation and deprotection were carried out in high yields.

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