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132885-30-4

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132885-30-4 Usage

Chemical class

Thioxodihydropyrimidinones

Derivative of

Thymine, a nucleobase found in DNA

Contains

a. Thioxo group
b. Hydroxyethoxy methyl group

Potential activities

a. Antiviral
b. Antitumor

Studied for

a. Treatment of viral infections
b. Treatment of cancer

Chemical structure

Promising candidate for further research and development

Potential use

As a therapeutic agent for viral infections and cancer treatment
These properties and specific content are based on the information provided, which highlights the compound's chemical class, derivative nature, structural components, and potential applications in the medical field.

Check Digit Verification of cas no

The CAS Registry Mumber 132885-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,8,8 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132885-30:
(8*1)+(7*3)+(6*2)+(5*8)+(4*8)+(3*5)+(2*3)+(1*0)=134
134 % 10 = 4
So 132885-30-4 is a valid CAS Registry Number.

132885-30-4SDS

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-hydroxyethoxymethyl)-5-methyl-2-sulfanylidenepyrimidin-4-one

1.2 Other means of identification

Product number -
Other names -

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:132885-30-4 SDS

132885-30-4Relevant articles and documents

A convenient one-pot synthesis of acyclonucleosides

Ubasawa,Takashima,Sekiya

, p. 142 - 143 (2007/10/02)

Bis(trimethylsilyl)pyrimidine bases were treated directly with 1,3-dioxolane (or 2-methyl-1,3-dioxolane), chlorotrimethylsilane and a metal iodide, such as KI or NaI, in acetonitrile at room temperature to afford acyclopyrimidine derivatives, including 2-thiopyrimidine derivatives, in good yields. Introduction of an acyclic chain into 2-thiopyrimidine bases, however, necessitated the use of 2 eq of the reagents.

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