Cas 437981-86-7,[Ni2S(SCH2CH3)(((CH3)2CH)2PCH2CH2P(CH(CH3)2)2)2](1+)*B(C6H5)4(1-)=[Ni2SSCH2CH3(((CH3)2CH)2PCH2CH2P(CH(CH3)2)2)2]B(C6H5)4

437981-86-7

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Basic information

Product Name: [Ni₂S(SCH₂CH₃)(((CH₃)2CH)2PCH₂CH₂P(CH(CH₃)2)2)2]⁽¹⁺⁾*B(C₆H₅)4^(1-)=[Ni₂SSCH₂CH₃(((CH₃)2CH)2PCH₂CH₂P(CH(CH₃)2)2)2]B(C₆H₅)4
Synonyms:
CAS NO:437981-86-7
Molecular Formula:
Molecular Weight: 1054.52
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: [Ni₂S(SCH₂CH₃)(((CH₃)2CH)2PCH₂CH₂P(CH(CH₃)2)2)2]⁽¹⁺⁾*B(C₆H₅)4^(1-)=[Ni₂SSCH₂CH₃(((CH₃)2CH)2PCH₂CH₂P(CH(CH₃)2)2)2]B(C₆H₅)4(CAS DataBase Reference)
NIST Chemistry Reference: [Ni₂S(SCH₂CH₃)(((CH₃)2CH)2PCH₂CH₂P(CH(CH₃)2)2)2]⁽¹⁺⁾*B(C₆H₅)4^(1-)=[Ni₂SSCH₂CH₃(((CH₃)2CH)2PCH₂CH₂P(CH(CH₃)2)2)2]B(C₆H₅)4(437981-86-7)
EPA Substance Registry System: [Ni₂S(SCH₂CH₃)(((CH₃)2CH)2PCH₂CH₂P(CH(CH₃)2)2)2]⁽¹⁺⁾*B(C₆H₅)4^(1-)=[Ni₂SSCH₂CH₃(((CH₃)2CH)2PCH₂CH₂P(CH(CH₃)2)2)2]B(C₆H₅)4(437981-86-7)

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: 437981-86-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 437981-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,7,9,8 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 437981-86:
(8*4)+(7*3)+(6*7)+(5*9)+(4*8)+(3*1)+(2*8)+(1*6)=197
197 % 10 = 7
So 437981-86-7 is a valid CAS Registry Number.

437981-86-7Upstream product

437981-86-7Downstream Products

437981-86-7Relevant academic research and scientific papers

Structure of [Ni(dippe)(μ-S)]2 and its reaction products. The nucleophilicity of the Ni2S2 fragment

Oster, Stephen S.,Lachicotte, Rene J.,Jones, William D.

, p. 118 - 127 (2008/10/08)

The dimer [(dippe)Ni(μ-S)]2 reacts with organic electrophiles to give the alkylated species [(dippe)2Ni2(μ-S)(μ-SR)]+. Stronger alkylating agents lead to double alkylation and cleavage of the dimer. Protonation

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