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131194-02-0

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131194-02-0 Usage

Chemical class

Pyrimidine derivative

Structural features

Contains a phenyl group
Contains a hydroxyethyl group

Potential applications

Pharmaceutical applications
Interaction with biological systems
Possible use in the development of new drugs or therapies

Biological activity

Interaction with enzymes or receptors

Research and industrial applications

Suitability for various research and industrial applications due to its properties

Structural characteristics

Presence of a 2,4(1H,3H)-dione group
Methyl group at the 5th position
Phenoxy group at the 6th position
(2-hydroxyethoxy)methyl group at the 1st position

Check Digit Verification of cas no

The CAS Registry Mumber 131194-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,1,9 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 131194-02:
(8*1)+(7*3)+(6*1)+(5*1)+(4*9)+(3*4)+(2*0)+(1*2)=90
90 % 10 = 0
So 131194-02-0 is a valid CAS Registry Number.

131194-02-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-hydroxyethoxymethyl)-5-methyl-6-phenoxypyrimidine-2,4-dione

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:131194-02-0 SDS

131194-02-0Downstream Products

131194-02-0Relevant articles and documents

A new class of HIV-1-specific 6-substituted acyclouridine derivatives: Synthesis and anti-HIV-1 activity of 5- or 6-substituted analogues of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT)

Tanaka,Baba,Hayakawa,Sakamaki,Miyasaka,Ubasawa,Takashima,Sekiya,Nitta,Shigeta,Walker,Balzarini,De Clercq

, p. 349 - 357 (2007/10/02)

A series of novel acyclouridine derivatives substituted at both the C-5 and C-6 positions were synthesized for the purpose of improving the activity of a recently reported HIV-1-specific lead, 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT). Prep

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