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CAS

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1393597-95-9

5-[N,N-bis(4-hexyloxyphenyl)amino]-2-(tri-n-butylstannyl)thiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1393597-95-9 Structure

  • Basic information

    1. Product Name: 5-[N,N-bis(4-hexyloxyphenyl)amino]-2-(tri-n-butylstannyl)thiophene
    2. Synonyms: 5-[N,N-bis(4-hexyloxyphenyl)amino]-2-(tri-n-butylstannyl)thiophene
    3. CAS NO:1393597-95-9
    4. Molecular Formula:
    5. Molecular Weight: 740.722
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1393597-95-9.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: 5-[N,N-bis(4-hexyloxyphenyl)amino]-2-(tri-n-butylstannyl)thiophene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-[N,N-bis(4-hexyloxyphenyl)amino]-2-(tri-n-butylstannyl)thiophene(1393597-95-9)
    11. EPA Substance Registry System: 5-[N,N-bis(4-hexyloxyphenyl)amino]-2-(tri-n-butylstannyl)thiophene(1393597-95-9)

  • 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: 1393597-95-9(Hazardous Substances Data)

1393597-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1393597-95-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,5,9 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1393597-95:
(9*1)+(8*3)+(7*9)+(6*3)+(5*5)+(4*9)+(3*7)+(2*9)+(1*5)=219
219 % 10 = 9
So 1393597-95-9 is a valid CAS Registry Number.

1393597-95-9Relevant articles and documents

Push-pull type meso -ester substituted BODIPY near-infrared dyes as contrast agents for photoacoustic imaging

Ni, Yong,Kannadorai, Ravi Kumar,Yu, Sidney W.-K.,Chang, Young-Tae,Wu, Jishan

, p. 4531 - 4535 (2017/07/10)

A series of push-pull type meso-ester substituted BODIPY dyes 1-4 with intense near-infrared absorption, largely enhanced photoacoustic (PA) activity and excellent photo-stability were synthesized. The impact of the electronic structure on the PA activity was also discussed. Moreover, the in vitro and in vivo PA imaging were investigated, which suggested a passive targeting capacity in the tumor site.

Fine-tuning the electronic structure of organic dyes for dye-sensitized solar cells

Gao, Peng,Tsao, Hoi Nok,Graetzel, Michael,Nazeeruddin, Mohammad K.

supporting information, p. 4330 - 4333 (2012/11/06)

A series of metal-free organic dyes exploiting different combinations of (hetero)cyclic linkers (benzene, thiophene, and thiazole) and bridges (4H-cyclopenta[2,1-b:3,4-b′]dithiophene (CPDT) and benzodithiophene (BDT)) as the central π-spacers were synthesized and characterized. Among them, the sensitizer containing the thiophene and CPDT showed the most broad incident photon-to-current conversion efficiency spectra, resulting in a solar energy conversion efficiency (η) of 6.6%.

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