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C6H3-2,6-(2,4,6-iPr3C6H2)2PB(4-dimethylaminopyridine)(2,2,6,6-tetramethylpiperidino) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 914095-19-5 Structure
  • Basic information

    1. Product Name: C6H3-2,6-(2,4,6-iPr3C6H2)2PB(4-dimethylaminopyridine)(2,2,6,6-tetramethylpiperidino)
    2. Synonyms:
    3. CAS NO:914095-19-5
    4. Molecular Formula:
    5. Molecular Weight: 785.988
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 914095-19-5.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: C6H3-2,6-(2,4,6-iPr3C6H2)2PB(4-dimethylaminopyridine)(2,2,6,6-tetramethylpiperidino)(CAS DataBase Reference)
    10. NIST Chemistry Reference: C6H3-2,6-(2,4,6-iPr3C6H2)2PB(4-dimethylaminopyridine)(2,2,6,6-tetramethylpiperidino)(914095-19-5)
    11. EPA Substance Registry System: C6H3-2,6-(2,4,6-iPr3C6H2)2PB(4-dimethylaminopyridine)(2,2,6,6-tetramethylpiperidino)(914095-19-5)
  • 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: 914095-19-5(Hazardous Substances Data)

914095-19-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 914095-19-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,0,9 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 914095-19:
(8*9)+(7*1)+(6*4)+(5*0)+(4*9)+(3*5)+(2*1)+(1*9)=165
165 % 10 = 5
So 914095-19-5 is a valid CAS Registry Number.

914095-19-5Relevant articles and documents

A donor-stabilization strategy for the preparation of compounds featuring P=B and As=B double bonds

Rivard, Eric,Merrill, W. Alexander,Fettinger, James C.,Power, Philip P.

, p. 3800 - 3802 (2006)

A new class of heavier group 15 compounds demonstrating multiple bonding with boron has been synthesized using a simple donor-stabilization protocol. The Royal Society of Chemistry 2006.

Boron-pnictogen multiple bonds: Donor-stabilized P=B and As=B bonds and a hindered iminoborane with a B-N triple bond

Rivard, Eric,Merrill, W. Alexander,Fettinger, James C.,Wolf, Robert,Spikes, Geoffrey H.,Power, Philip P.

, p. 2971 - 2978 (2008/10/09)

Reaction of the hindered phosphino- and arsinoboranes, Ar*Pn(H)-B(Br) Tmp (Ar* = -C6H3-2,6-(C6H 2-2,4,6-iPr3)2; Tmp = 2,2,6,6-tetramethylpiperidino; Pn = P and As, 1 and 3, respectively) with 4-dimethylaminopyridine, DMAP, afforded the boranylidenephosphane and arsane, Ar*Pn=B(DMAP)Tmp (Pn = P and As, 2 and 4) as deep red-purple solids. The analogous aminoboranes Ar′N(H)-B(X)Tmp (Ar′ = -C6H 3-2,6-(C6H2-2,4,6-Me3)2; X = Cl and Br; 5 and 6) did not display any reactivity with DMAP, but in the presence of the amide base, Na[N(SiMe3)2], the clean formation of the uncomplexed iminoborane Ar′N≡BTmP (7) was observed. Attempts to generate an Sb=B bond were unsuccessful, as the required stibinoborane precursor, Ar*Sb(H)-B(Br)Tmp, could not be prepared; in place of clean Sb-B bond formation, the reduced product Ar*Sb=SbAr* was obtained. All compounds were characterized spectroscopically, and the X-ray crystal structures of 1, 2, 4, 6, and 7 were determined.

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