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  • 1391852-05-3 Structure
  • Basic information

    1. Product Name: C27H20BF2N3
    2. Synonyms: C27H20BF2N3
    3. CAS NO:1391852-05-3
    4. Molecular Formula:
    5. Molecular Weight: 435.284
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1391852-05-3.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: C27H20BF2N3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C27H20BF2N3(1391852-05-3)
    11. EPA Substance Registry System: C27H20BF2N3(1391852-05-3)
  • 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: 1391852-05-3(Hazardous Substances Data)

1391852-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1391852-05-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,1,8,5 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1391852-05:
(9*1)+(8*3)+(7*9)+(6*1)+(5*8)+(4*5)+(3*2)+(2*0)+(1*5)=173
173 % 10 = 3
So 1391852-05-3 is a valid CAS Registry Number.

1391852-05-3Downstream Products

1391852-05-3Relevant articles and documents

Isoindole-BODIPY dyes as red to near-infrared fluorophores

Yu, Changjiang,Xu, Yajun,Jiao, Lijuan,Zhou, Jinyuan,Wang, Zhaoyun,Hao, Erhong

, p. 6437 - 6442 (2012)

Three-in-one go: One-pot synthesis of isoindole-BODIPY dyes was developed based on nucleophilic substitution (SNAr) reactions of in situ formed chlorinated dipyrromethene by pyrrole. These dyes have long wavelengths, sharp absorption and fluorescence, high fluorescence quantum yields, and high photostability. The wavelength is finely tunable over a wide range (590-714 nm) by variation of substituent groups and functionalization (see scheme). Copyright

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