Cas 211186-98-0,ZnC20N4H2(CH3)4(C6H13)4[C6H3(C(CH3)3)2]C6H4C3O2BH5C14N2H4(O)4C6H13

211186-98-0

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Basic information

Product Name: ZnC₂₀N₄H₂(CH₃)4(C₆H₁₃)4[C₆H₃(C(CH₃)3)2]C₆H₄C₃O₂BH₅C₁₄N₂H₄(O)4C₆H₁₃
Synonyms: ZnC₂₀N₄H₂(CH₃)4(C₆H₁₃)4[C₆H₃(C(CH₃)3)2]C₆H₄C₃O₂BH₅C₁₄N₂H₄(O)4C₆H₁₃
CAS NO:211186-98-0
Molecular Formula:
Molecular Weight: 1463.14
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: ZnC₂₀N₄H₂(CH₃)4(C₆H₁₃)4[C₆H₃(C(CH₃)3)2]C₆H₄C₃O₂BH₅C₁₄N₂H₄(O)4C₆H₁₃(CAS DataBase Reference)
NIST Chemistry Reference: ZnC₂₀N₄H₂(CH₃)4(C₆H₁₃)4[C₆H₃(C(CH₃)3)2]C₆H₄C₃O₂BH₅C₁₄N₂H₄(O)4C₆H₁₃(211186-98-0)
EPA Substance Registry System: ZnC₂₀N₄H₂(CH₃)4(C₆H₁₃)4[C₆H₃(C(CH₃)3)2]C₆H₄C₃O₂BH₅C₁₄N₂H₄(O)4C₆H₁₃(211186-98-0)

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: 211186-98-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 211186-98-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,1,8 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 211186-98:
(8*2)+(7*1)+(6*1)+(5*1)+(4*8)+(3*6)+(2*9)+(1*8)=110
110 % 10 = 0
So 211186-98-0 is a valid CAS Registry Number.

211186-98-0Upstream product

171521-54-3 2-Hexyl-7-(2-hydroxy-1-hydroxymethyl-ethyl)-benzo[lmn][3,8]phenanthroline-1,3,6,8-tetraone

211186-98-0Downstream Products

211186-98-0Relevant academic research and scientific papers

Coordination control of intramolecular electron transfer in boronate ester-bridged donor-acceptor molecules

Shiratori, Hideo,Ohno, Takeshi,Nozaki, Koichi,Yamazaki, Iwao,Nishimura, Yoshinobu,Osuka, Atsuhiro

, p. 1539 - 1540 (1998)

Acid-base reaction at the bridge in a donor-acceptor molecule can influence intramolecular electron-transfer reactions; this has been demonstrated in boronate ester bridged zinc porphyrin-diimide dyads in which intramolecular electron transfer reaction has been completely suppressed by coordination of F- on the bridge boron.

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