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108047-30-9

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  • 108047-30-9 Structure

  • Basic information

    1. Product Name: 3-methyl-5-nitro-1-(p-nitrophenyl)uracil
    2. Synonyms: 3-methyl-5-nitro-1-(p-nitrophenyl)uracil
    3. CAS NO:108047-30-9
    4. Molecular Formula:
    5. Molecular Weight: 292.208
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108047-30-9.mol
    9. Article Data: 4

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-methyl-5-nitro-1-(p-nitrophenyl)uracil(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-methyl-5-nitro-1-(p-nitrophenyl)uracil(108047-30-9)
    11. EPA Substance Registry System: 3-methyl-5-nitro-1-(p-nitrophenyl)uracil(108047-30-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 108047-30-9(Hazardous Substances Data)

108047-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108047-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,0,4 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 108047-30:
(8*1)+(7*0)+(6*8)+(5*0)+(4*4)+(3*7)+(2*3)+(1*0)=99
99 % 10 = 9
So 108047-30-9 is a valid CAS Registry Number.

108047-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1-(4-nitrophenyl)-5-nitrouracil

1.2 Other means of identification

Product number -
Other names .3-methyl-5-nitro-1-(p-nirophenyl)uracil

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:108047-30-9 SDS

108047-30-9Relevant articles and documents

N-Functionalization of uracil derivatives: Synthesis of chiral 2-(3-methyl-5-nitro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)alkanoic acids and their methyl esters

Gondela, Andrzej,Walczak, Krzysztof

, p. 2107 - 2112 (2005)

3-Methyl-5-nitro-1-(4-nitrophenyl)uracil has been obtained by regioselective arylation of uracil using 4-nitrofluorobenzene, followed by methylation at the nitrogen atom N-3 and subsequent nitration of the uracil ring. 3-Methyl-5-nitro-1-(4-nitrophenyl)ur

Novel Reaction of Uracil Derivatives Possessing Electron-withdrawing Groups at the 5-Position with Amines: Exchange Reaction between the N1-Portion of Uracils and Amines

Hirota, Kosaku,Kitade, Yukio,Sajiki, Hironao,Maki, Yoshifumi,Yogo, Motoi

, p. 367 - 373 (2007/10/02)

The reaction of 1,3-disubstituted uracils possessing an electron-withdrawing group such as nitro, carbamoyl, and cyano at 5-position with primary amines resulted in the exchange of the N1-portion of the uracil ring with the amine moiety.The exchange reactions were influenced by the nature of substituents at the 5- and N1-position.The reaction sequence is explained in terms of addition, ring-opening, and ring-closure.

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