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  • 1427269-37-1 Structure
  • Basic information

    1. Product Name: C43H44N12O13P2
    2. Synonyms:
    3. CAS NO:1427269-37-1
    4. Molecular Formula:
    5. Molecular Weight: 998.842
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1427269-37-1.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: C43H44N12O13P2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C43H44N12O13P2(1427269-37-1)
    11. EPA Substance Registry System: C43H44N12O13P2(1427269-37-1)
  • 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: 1427269-37-1(Hazardous Substances Data)

1427269-37-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1427269-37-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,2,6 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1427269-37:
(9*1)+(8*4)+(7*2)+(6*7)+(5*2)+(4*6)+(3*9)+(2*3)+(1*7)=171
171 % 10 = 1
So 1427269-37-1 is a valid CAS Registry Number.

1427269-37-1Upstream product

1427269-37-1Downstream Products

1427269-37-1Relevant articles and documents

Synthesis of 2'-modified cyclic bis(3'5') diadenylic acids (c-di-AMPs) and their promotion of cell division in a freshwater green alga

Tezuka, Takafumi,Suzuki, Noritaka,Ishida, Keigo,Oyama, Kin-Ichi,Aoki, Setsuyuki,Tsukamoto, Masaki

, p. 1723 - 1725 (2012)

Three 2'-modified cyclic bis(3'5') diadenylic acids (c-di-AMPs) were synthesized from commercially available adenosine phosphoramidites and the effects of c-di-AMP derivatives on the cell division of Chlamydomonas reinhardtii, a kind of freshwater green algae, were investigated. This structureactivity relationship study suggests that the di(2'-O-methyl)-c-di-AMP showed the highest activity and that 2'-substituents influenced the cell division of C. reinhardtii.

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