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136160-18-4

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136160-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136160-18-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,1,6 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 136160-18:
(8*1)+(7*3)+(6*6)+(5*1)+(4*6)+(3*0)+(2*1)+(1*8)=104
104 % 10 = 4
So 136160-18-4 is a valid CAS Registry Number.

136160-18-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-6-phenylsulfanyl-1H-pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-methyl-6-(phenylthio)pyrimidine-2,4(1H,3H)-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:136160-18-4 SDS

136160-18-4Relevant articles and documents

Functionalization of unprotected uracil derivatives using the halogen - Magnesium exchange

Kopp, Felix,Knoechel, Paul

, p. 1639 - 1641 (2008/02/02)

The reaction of commercially available 5-iodouracil with 2 equiv of MeMgCl in the presence of LiCl, followed by the addition of i-PrMgCl-LiCl, provides the corresponding trimagnesiated species, which reacts with various electrophiles to give selectively 5

Pyrimidine derivatives and anti-viral agent containing the same as active ingredient thereof

-

, (2008/06/13)

The disclosure concerns pyrimidine derivatives represented by the following general formulas [I] and [I'] and having antiviral activity, particularly antiretroviral activity such as anti-HIV activity: STR1 and pharmaceutical compositions having antiviral

Synthesis and Antiviral Activity of Deoxy Analogs of 1--6-(phenylthio)thymine (HEPT) as Potent and Selective Anti-HIV-1 Agents

Tanaka, Hiromichi,Takashima, Hideaki,Ubasawa, Masaru,Sekiya, Kouichi,Nitta, Issei,et al.

, p. 4713 - 4719 (2007/10/02)

The effect of substitution in the acyclic structure of 1--6-(phenylthio)thymine (HEPT) on anti-HIV-1 activity was investigated by synthesizing a series of deoxy analogs and related compounds.Preparation of 1-(2-alkyloxyethoxy)met

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