Welcome to LookChem.com Sign In|Join Free
  • or
N-(6-chloro-3-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)formamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89380-01-8

Post Buying Request

89380-01-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

89380-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89380-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,8 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89380-01:
(7*8)+(6*9)+(5*3)+(4*8)+(3*0)+(2*0)+(1*1)=158
158 % 10 = 8
So 89380-01-8 is a valid CAS Registry Number.

89380-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(6-chloro-3-methyl-2,4-dioxo-1H-pyrimidin-5-yl)formamide

1.2 Other means of identification

Product number -
Other names 6-chloro-5-formylamino-3-methyl-1H-pyrimidine-2,4-dione

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:89380-01-8 SDS

89380-01-8Relevant academic research and scientific papers

Convenient synthesis of toxoflavin that targets β-catenin/TCF4 signaling activities

Mao, Yongjun,Tian, Wang,Huang, Ziwei,An, Jing

, p. 594 - 597 (2014/06/10)

A rapid and improved route for synthesis of toxoflavin, an antibiotic and antitumor agent, is described. The method uses easily obtained materials and simple and practical reactions, including chlorination, condensation, and diazotization to produce toxoflavin in five steps with 14.2% yield and 98.6% purity (HPLC). This synthetic toxoflavin effectively inhibited β-catenin/Tcf4 driven TOP-luciferase activity with an IC50 of less than 0.5 μM and induced colon cancer cell death in a dose-dependent manner with an IC50 of 0.29 μM.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 89380-01-8