Cas 1287239-95-5,B(O)N2C3H(CH3)(CH2)(C6H3(CH(CH3)2)2)2(1-)*N2C3H(CH3)2(CH(CH3)2)2(1+)=BO(C40H61N4)

1287239-95-5

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Basic information

Product Name: B(O)N₂C₃H(CH₃)(CH₂)(C₆H₃(CH(CH₃)2)2)2^(1-)*N₂C₃H(CH₃)2(CH(CH₃)2)2⁽¹⁺⁾=BO(C₄₀H₆₁N₄)
Synonyms: B(O)N₂C₃H(CH₃)(CH₂)(C₆H₃(CH(CH₃)2)2)2^(1-)*N₂C₃H(CH₃)2(CH(CH₃)2)2⁽¹⁺⁾=BO(C₄₀H₆₁N₄)
CAS NO:1287239-95-5
Molecular Formula:
Molecular Weight: 624.762
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: B(O)N₂C₃H(CH₃)(CH₂)(C₆H₃(CH(CH₃)2)2)2^(1-)*N₂C₃H(CH₃)2(CH(CH₃)2)2⁽¹⁺⁾=BO(C₄₀H₆₁N₄)(CAS DataBase Reference)
NIST Chemistry Reference: B(O)N₂C₃H(CH₃)(CH₂)(C₆H₃(CH(CH₃)2)2)2^(1-)*N₂C₃H(CH₃)2(CH(CH₃)2)2⁽¹⁺⁾=BO(C₄₀H₆₁N₄)(1287239-95-5)
EPA Substance Registry System: B(O)N₂C₃H(CH₃)(CH₂)(C₆H₃(CH(CH₃)2)2)2^(1-)*N₂C₃H(CH₃)2(CH(CH₃)2)2⁽¹⁺⁾=BO(C₄₀H₆₁N₄)(1287239-95-5)

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: 1287239-95-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1287239-95-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,7,2,3 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1287239-95:
(9*1)+(8*2)+(7*8)+(6*7)+(5*2)+(4*3)+(3*9)+(2*9)+(1*5)=195
195 % 10 = 5
So 1287239-95-5 is a valid CAS Registry Number.

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1287239-95-5Relevant academic research and scientific papers

Comparison of anionic and Lewis acid stabilized N-heterocyclic oxoboranes: Their facile synthesis from a borinic acid

Wang, Yan,Hu, Hongfan,Zhang, Jianying,Cui, Chunming

supporting information; experimental part, p. 2816 - 2819 (2011/06/10)

Have it B=Oth ways: Metal-free anionic oxoboranes and Lewis acid stabilized oxoboranes that feature a formal B-O double bond can be conveniently obtained from an N-heterocyclic borinic acid in the presences of N-heterocyclic carbenes (NHCs) and Lewis acids, respectively (see picture). Copyright

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