Cas 359856-69-2,5α,15β-bis(2-benzoylaminophenyl)-10α,20β-bis(2-(N,N-dimethylaminomethylcarbonylamino)phenyl)porphyrinatozinc(II)

359856-69-2

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Basic information

Product Name: 5α,15β-bis(2-benzoylaminophenyl)-10α,20β-bis(2-(N,N-dimethylaminomethylcarbonylamino)phenyl)porphyrinatozinc(II)
Synonyms:
CAS NO:359856-69-2
Molecular Formula:
Molecular Weight: 1116.61
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: 5α,15β-bis(2-benzoylaminophenyl)-10α,20β-bis(2-(N,N-dimethylaminomethylcarbonylamino)phenyl)porphyrinatozinc(II)(CAS DataBase Reference)
NIST Chemistry Reference: 5α,15β-bis(2-benzoylaminophenyl)-10α,20β-bis(2-(N,N-dimethylaminomethylcarbonylamino)phenyl)porphyrinatozinc(II)(359856-69-2)
EPA Substance Registry System: 5α,15β-bis(2-benzoylaminophenyl)-10α,20β-bis(2-(N,N-dimethylaminomethylcarbonylamino)phenyl)porphyrinatozinc(II)(359856-69-2)

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: 359856-69-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 359856-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,9,8,5 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 359856-69:
(8*3)+(7*5)+(6*9)+(5*8)+(4*5)+(3*6)+(2*6)+(1*9)=212
212 % 10 = 2
So 359856-69-2 is a valid CAS Registry Number.

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359856-69-2Relevant academic research and scientific papers

Water-soluble zinc porphyrins as receptors for amino carboxylates

Imai, Hiroyasu,Misawa, Kensuke,Munakata, Hiroki,Uemori, Yoshio

, p. 688 - 689 (2001)

Water-soluble zinc porphyrins bearing an ammonium group and a phenyl or tertiary butyl group above each porphyrin plane were designed and synthesized. Binding data for amino carboxylates in aqueous solution suggested that these porphyrins recognize the carboxylates on the basis of coordinative, Coulomb, and hydrophobic interactions and that a chiral recognition phenomenon for glycyl-tryptophan anion is derived from the cooperation of these interactions.

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