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2-(5,5-dimethyltetrahydrofuran-2-yl)-5,8-dihydroxynaphthalene-1,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64981-70-0

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64981-70-0 Usage

Molecular structure

Consists of a naphthalene-1,4-dione core, a tetrahydrofuran ring, and two hydroxyl groups.

Type of compound

Synthetic organic compound.

Potential applications

Therapeutic uses, particularly in medicinal chemistry and drug development.

Biological activities

The complex structure suggests a range of potential biological activities, though further research is needed to understand them fully.

Research necessity

Further studies are required to explore the compound's potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 64981-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,8 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64981-70:
(7*6)+(6*4)+(5*9)+(4*8)+(3*1)+(2*7)+(1*0)=160
160 % 10 = 0
So 64981-70-0 is a valid CAS Registry Number.

64981-70-0SDS

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 Cycloalkannin

1.2 Other means of identification

Product number -
Other names CYCLO(-D-TYR-ARG-GLY-ASP-CYS (CARBOXYMETHYL)-OH) SULFOXIDE

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:64981-70-0 SDS

64981-70-0Downstream Products

64981-70-0Relevant academic research and scientific papers

Asymmetric synthesis and antitumor activity of cycloalkanin

Wu, Xihan,Xu, Liang,Cai, Junchao

, p. 2635 - 2638 (2007/10/03)

Cycloalkanin was accessible by a practical and efficient asymmetric synthesis. The chiral center of the target is introduced via an asymmetric C-arylation of chiral aldehyde in high de. The synthesized cycloalkanin was shown to be significantly active against P388 cell line as assayed by in vitro MTT method.

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