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dicyclohexylphosphane selenide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 128337-01-9 Structure
  • Basic information

    1. Product Name: dicyclohexylphosphane selenide
    2. Synonyms: dicyclohexylphosphane selenide
    3. CAS NO:128337-01-9
    4. Molecular Formula:
    5. Molecular Weight: 277.248
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 128337-01-9.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: dicyclohexylphosphane selenide(CAS DataBase Reference)
    10. NIST Chemistry Reference: dicyclohexylphosphane selenide(128337-01-9)
    11. EPA Substance Registry System: dicyclohexylphosphane selenide(128337-01-9)
  • 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: 128337-01-9(Hazardous Substances Data)

128337-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128337-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,3,3 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 128337-01:
(8*1)+(7*2)+(6*8)+(5*3)+(4*3)+(3*7)+(2*0)+(1*1)=119
119 % 10 = 9
So 128337-01-9 is a valid CAS Registry Number.

128337-01-9Upstream product

128337-01-9Relevant articles and documents

The formation mechanism of binary semiconductor nanomaterials: Shared by single-source and dual-source precursor approaches

Yu, Kui,Liu, Xiangyang,Zeng, Qun,Yang, Mingli,Ouyang, Jianying,Wang, Xinqin,Tao, Ye

, p. 11034 - 11039 (2013)

One thing in common: The formation of binary colloidal semiconductor nanocrystals from single- (M(EEPPh2)n) and dual-source precursors (metal carboxylates M(OOCR)n and phosphine chalcogenides such as E=PHPh2) is found to proceed through a common mechanism. For CdSe as a model system 31Pa NMR spectroscopy and DFT calculations support a reaction mechanism which includes numerous metathesis equilibriums and Se exchange reactions. Copyright

Transition-metal-mediated cyclocotrimerization of selenophosphinites with activated alkynes

Lindner, Ekkehard,Bosch, Elke,Fawzi, Riad,Steimann, Manfred,Mayer, Hermann A.,Gierling, Karlheinz

, p. 945 - 951 (2007/10/03)

Selenophosphinito complexes (OC)4Mn(η2-Se...PR1/2) (2a, b) [R1 = eye-Hex (a), iBu (b)] are formed by the reaction of BrMn(CO)5 with the phosphane selenides R2HPSe (1a, b) in the presence of the auxiliary base Et(iPr)2

NOVEL ANIONIC CHALCOGENO LIGANDS. TELLUROPHOSPHINITES R2PTe- AND CHALCOGENOTELLUROPHOSPHINATES R2P(Ch)Te-

Bildstein, Benno,Sladky, Fritz

, p. 341 - 347 (2007/10/02)

Elemental tellurium reacts with diorganylphosphides R2P- to give tellurophosphinites R2PTe- and with chalcogenophosphinites R2PCh- to give chalcogenotellurophosphinates R2P(Ch)Te- R = C6H11, C6H5; Ch = O,S,Se,T

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