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1041467-70-2

9-(2-hydroxy-1-phenylethyl)guanine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1041467-70-2 Structure

  • Basic information

    1. Product Name: 9-(2-hydroxy-1-phenylethyl)guanine
    2. Synonyms: 9-(2-hydroxy-1-phenylethyl)guanine
    3. CAS NO:1041467-70-2
    4. Molecular Formula:
    5. Molecular Weight: 271.279
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1041467-70-2.mol

  • 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: 9-(2-hydroxy-1-phenylethyl)guanine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9-(2-hydroxy-1-phenylethyl)guanine(1041467-70-2)
    11. EPA Substance Registry System: 9-(2-hydroxy-1-phenylethyl)guanine(1041467-70-2)

  • 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: 1041467-70-2(Hazardous Substances Data)

1041467-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1041467-70-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,1,4,6 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1041467-70:
(9*1)+(8*0)+(7*4)+(6*1)+(5*4)+(4*6)+(3*7)+(2*7)+(1*0)=122
122 % 10 = 2
So 1041467-70-2 is a valid CAS Registry Number.

1041467-70-2Downstream Products

1041467-70-2Relevant articles and documents

Synthesis of 3-(2-hydroxy-1-phenylethyl)- and 3-(2-hydroxy-2-phenylethyl) adenine, DNA adducts derived from styrene

Krouzelka, Jan,Linhart, Igor,Tobrman, Tomas

, p. 789 - 795 (2008)

(Chemical Equation Presented) 3-(2-Hydroxy-2-phenylethyl)- and 3-(2-hydroxy-1-phenylethyl)adenine, DNA adducts derived from styrene, along with their 9-substituted analogues were prepared by alkylation of 8-bromoadenine with corresponding allyl-protected bromohydrins followed by a new deallylation procedure using tetrakis(triphenylphosphine)palladium catalyzed reductive cleavage by poly(methylhydrosiloxane) in the presence of p-toluenesulphonic acid. This novel procedure proved to be useful for purine derivatives, which were resistant to other deallylation protocols. Structure of positional isomers was assigned using 2D NMR experiments HMBC and HMQC.

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