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116301-02-1

(S)-P3-1-(2-nitrophenyl)ethyladenosin triphosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 116301-02-1 Structure

  • Basic information

    1. Product Name: (S)-P3-1-(2-nitrophenyl)ethyladenosin triphosphate
    2. Synonyms:
    3. CAS NO:116301-02-1
    4. Molecular Formula:
    5. Molecular Weight: 656.333
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116301-02-1.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: (S)-P3-1-(2-nitrophenyl)ethyladenosin triphosphate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-P3-1-(2-nitrophenyl)ethyladenosin triphosphate(116301-02-1)
    11. EPA Substance Registry System: (S)-P3-1-(2-nitrophenyl)ethyladenosin triphosphate(116301-02-1)

  • 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: 116301-02-1(Hazardous Substances Data)

116301-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116301-02-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,3,0 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 116301-02:
(8*1)+(7*1)+(6*6)+(5*3)+(4*0)+(3*1)+(2*0)+(1*2)=71
71 % 10 = 1
So 116301-02-1 is a valid CAS Registry Number.

116301-02-1Downstream Products

116301-02-1Relevant articles and documents

Synthesis and Absolute Sterochemistry of the Two Diasteromers of P3-1-(2-Nitrophenyl)ethyl Adenosine Triphosphate ("Caged" ATP)

Corrie, John E. T.,Reid, Gordon P.,Trentham, David R.,Hursthouse, Michael B.,Mazid, Muhammed A.

, p. 1015 - 1020 (1992)

1-(2-Nitrophenyl)ethanol was resolved by fractional crystallisation of its diastereoisomeric (1S)-camphanates.The absolute stereochemistry of the (S)-alcohol was determined using the Horeau kinetic resolution procedure, and subsequently confirmed by X-ray crystallography of its (1S)-camphanate ester.The resolved alcohols were converted to (R)- and (S)-1-(2-nitrophenyl)ethyl phosphates, each of which was condensed with adenosine diphosphate to give the (R)- and (S)-1-(2-nitrophenyl)ethyl P3-esters of adenosine triphosphate.

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