Cas 282117-16-2,HPt(NC5H4C(C6H5)NC6H4NC6H4O2C4H6(C2H5)(CHCH2))(1+)*CF3SO3(1-)=[HPt(NC5H4CC6H5NC6H4NC6H4O2C4H6(C2H5)(CHCH2))]CF3SO3

282117-16-2

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Basic information

Product Name: HPt(NC₅H₄C(C₆H₅)NC₆H₄NC₆H₄O₂C₄H₆(C₂H₅)(CHCH₂))⁽¹⁺⁾*CF₃SO₃^(1-)=[HPt(NC₅H₄CC₆H₅NC₆H₄NC₆H₄O₂C₄H₆(C₂H₅)(CHCH₂))]CF₃SO₃
Synonyms: HPt(NC₅H₄C(C₆H₅)NC₆H₄NC₆H₄O₂C₄H₆(C₂H₅)(CHCH₂))⁽¹⁺⁾*CF₃SO₃^(1-)=[HPt(NC₅H₄CC₆H₅NC₆H₄NC₆H₄O₂C₄H₆(C₂H₅)(CHCH₂))]CF₃SO₃
CAS NO:282117-16-2
Molecular Formula:
Molecular Weight: 834.775
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: HPt(NC₅H₄C(C₆H₅)NC₆H₄NC₆H₄O₂C₄H₆(C₂H₅)(CHCH₂))⁽¹⁺⁾*CF₃SO₃^(1-)=[HPt(NC₅H₄CC₆H₅NC₆H₄NC₆H₄O₂C₄H₆(C₂H₅)(CHCH₂))]CF₃SO₃(CAS DataBase Reference)
NIST Chemistry Reference: HPt(NC₅H₄C(C₆H₅)NC₆H₄NC₆H₄O₂C₄H₆(C₂H₅)(CHCH₂))⁽¹⁺⁾*CF₃SO₃^(1-)=[HPt(NC₅H₄CC₆H₅NC₆H₄NC₆H₄O₂C₄H₆(C₂H₅)(CHCH₂))]CF₃SO₃(282117-16-2)
EPA Substance Registry System: HPt(NC₅H₄C(C₆H₅)NC₆H₄NC₆H₄O₂C₄H₆(C₂H₅)(CHCH₂))⁽¹⁺⁾*CF₃SO₃^(1-)=[HPt(NC₅H₄CC₆H₅NC₆H₄NC₆H₄O₂C₄H₆(C₂H₅)(CHCH₂))]CF₃SO₃(282117-16-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 282117-16-2(Hazardous Substances Data)

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282117-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 282117-16-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,2,1,1 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 282117-16:
(8*2)+(7*8)+(6*2)+(5*1)+(4*1)+(3*7)+(2*1)+(1*6)=122
122 % 10 = 2
So 282117-16-2 is a valid CAS Registry Number.

282117-16-2Upstream product

282117-20-8 (CH₃)Pt(NC₅H₄C(C₆H₅)NC₆H₄NC₄H(COOCH₃)C₄H₆(C₂H₅)2)⁽¹⁺⁾*CF₃SO₃^(1-)=[CH₃Pt(NC₅H₄C(C₆H₅)NC₆H₄NC₄H(COOCH₃)C₄H₆(C₂H₅)2)]CF₃SO₃

282117-16-2Downstream Products

443797-72-6 [ClPt(NC₅H₄C(C₆H₅)NC₆H₄NC₆H₄O₂C₄H₆(C₂H₅)(C₂H₄))]

282117-16-2Relevant academic research and scientific papers

Total synthesis of (-)-rhazinilam: Asymmetric C-H bond activation via the use of a chiral auxiliary

Johnson, James A.,Li, Ning,Sames, Dalibor

, p. 6900 - 6903 (2002)

The antitumor agent (-)-rhazinilam was synthesized in three major steps, namely the pyrrole synthesis, selective C-H bond activation, and direct macrolactam formation. The key step involved asymmetric C-H bond functionalization (dehydrogenation) of the di

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