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322732-57-0

2-[5-(4-Methoxyphenyl)pyrimidin-2-yl]ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 322732-57-0 Structure

  • Basic information

    1. Product Name: 2-[5-(4-Methoxyphenyl)pyrimidin-2-yl]ethanol
    2. Synonyms: 2-pyrimidineethanol, 5-(4-methoxyphenyl)-
    3. CAS NO:322732-57-0
    4. Molecular Formula: C13H14N2O2
    5. Molecular Weight: 230.2625
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 322732-57-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 405.82°C at 760 mmHg
    3. Flash Point: 199.233°C
    4. Appearance: N/A
    5. Density: 1.178g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.577
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-[5-(4-Methoxyphenyl)pyrimidin-2-yl]ethanol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-[5-(4-Methoxyphenyl)pyrimidin-2-yl]ethanol(322732-57-0)
    12. EPA Substance Registry System: 2-[5-(4-Methoxyphenyl)pyrimidin-2-yl]ethanol(322732-57-0)

  • 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: 322732-57-0(Hazardous Substances Data)

322732-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 322732-57-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,2,7,3 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 322732-57:
(8*3)+(7*2)+(6*2)+(5*7)+(4*3)+(3*2)+(2*5)+(1*7)=120
120 % 10 = 0
So 322732-57-0 is a valid CAS Registry Number.

322732-57-0Relevant articles and documents

β-Heteroarylethyl Groups - New Phosphate-Protecting Groups for Phosphotriester Chemistry

Reiner, Tilman,Kvasyuk, Evgeny,Pfleiderer, Wolfgang

, p. 3053 - 3063 (2007/10/03)

The β-heteroaryl-substituted ethanols 6-10 were synthesized and, together with pyridine-2-ethanols and pyridine-4-ethanols, were tested as a new type of phosphate-protecting groups in the synthesis of oligonucleotides by the phosphotriester approach. The synthesis of 5'-O-(monomethoxytrityl)thymidine 3'-(β-heteroarylethyl 2,5-dichlorophenyl phosphates) 13-17 and 21 provided useful monomeric building blocks in which the various blocking groups could be removed selectively by acid (MeOTr), oximate (2,5-dichlorophenyl phosphate), and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (heteroarylethyl phosphate) treatment. The new, fully blocked dimers 38-41, with β-heteroarylethyl protecting groups in the phosphate moiety, were synthesized. The β-heteroarylethyl groups show a broad range of stability towards base treatment in aprotic solvents depending upon the activation of the H-C(β) atoms by the heterocyclic moiety.

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