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110960-75-3

ETHYL-4-ETHYL-5-PYRIMIDINE CARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 110960-75-3 Structure

  • Basic information

    1. Product Name: ETHYL-4-ETHYL-5-PYRIMIDINE CARBOXYLATE
    2. Synonyms: ETHYL-4-ETHYL-5-PYRIMIDINE CARBOXYLATE
    3. CAS NO:110960-75-3
    4. Molecular Formula: C9H12N2O2
    5. Molecular Weight: 180.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 110960-75-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 292.5°Cat760mmHg
    3. Flash Point: 130.7°C
    4. Appearance: /
    5. Density: 1.104g/cm3
    6. Vapor Pressure: 0.00182mmHg at 25°C
    7. Refractive Index: 1.505
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: ETHYL-4-ETHYL-5-PYRIMIDINE CARBOXYLATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: ETHYL-4-ETHYL-5-PYRIMIDINE CARBOXYLATE(110960-75-3)
    12. EPA Substance Registry System: ETHYL-4-ETHYL-5-PYRIMIDINE CARBOXYLATE(110960-75-3)

  • 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: 110960-75-3(Hazardous Substances Data)

110960-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110960-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,9,6 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 110960-75:
(8*1)+(7*1)+(6*0)+(5*9)+(4*6)+(3*0)+(2*7)+(1*5)=103
103 % 10 = 3
So 110960-75-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O2/c1-3-8-7(5-10-6-11-8)9(12)13-4-2/h5-6H,3-4H2,1-2H3

110960-75-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-ethylpyrimidine-5-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 4-ethyl-5-pyrimidine carboxylate

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:110960-75-3 SDS

110960-75-3Downstream Products

110960-75-3Relevant articles and documents

Benzylic Fluorination of Aza-Heterocycles Induced by Single-Electron Transfer to Selectfluor

Danahy, Kelley E.,Cooper, Julian C.,Van Humbeck, Jeffrey F.

, p. 5134 - 5138 (2018)

A selective and mild method for the benzylic fluorination of aromatic azaheterocycles with Selectfluor is described. These reactions take place by a previously unreported mechanism, in which electron transfer from the heterocyclic substrate to the electrophilic fluorinating agent Selectfluor eventually yields a benzylic radical, thus leading to the desired C?F bond formation. This mechanism enables high intra- and intermolecular selectivity for aza-heterocycles over other benzylic components with similar C?H bond-dissociation energies.

TWO PATHS FOR THE FORMATION OF PYRIMIDINES FROM sym-TRIAZINE

Gromov, S. P.,Yashunskii, D. V.,Sagitullin, R. S.,Bundel, Yu. G.

, p. 1054 - 1059 (2007/10/02)

The reaction of sym-triazine with the hydrochlorides of N-unsubstituted enaminones gives mixtures of 4-alkyl-5-acyl(ethoxycarbonyl)pyrimidines and 2,6-dialkyl-3,5-diacyl(ethoxycarbonyl)pyridines.The reaction mechanism was studied by means of the 15N-labelled compounds.

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