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117733-47-8

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117733-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117733-47-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,7,3 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 117733-47:
(8*1)+(7*1)+(6*7)+(5*7)+(4*3)+(3*3)+(2*4)+(1*7)=128
128 % 10 = 8
So 117733-47-8 is a valid CAS Registry Number.

117733-47-8Downstream Products

117733-47-8Relevant articles and documents

COMPOSITION, PHOTOELECTRIC CONVERSION ELEMENT, AND IMAGING DEVICE

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Paragraph 0249; 0253-0254, (2021/08/06)

A composition contains a naphthalocyanine derivative represented by the following formula: where R1 to R8 are independently an alkyl group and R9 to R12 are independently an aryl group, and at least one hydrogen atom in at least one selected from the group consisting of R9, R10, R11, and R12 is substituted by an electron-withdrawing group.

COMPOSITION, AND PHOTOELECTRIC CONVERSION ELEMENT AND IMAGING DEVICE THAT EMPLOY THE SAME

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Paragraph 0152; 0158; 0159; 0160, (2019/01/23)

PROBLEM TO BE SOLVED: To provide a composition, a photoelectric conversion element and an imaging device which have high light absorption characteristics in the near-infrared region and exhibit high photoelectric conversion efficiency. SOLUTION: A composition contains a compound represented by the general formula in the figure, where M represents either Si or Sn; R1 to R8 each independently represent an alkyl group containing three or less carbon atoms; and R9 to R14 each independently represent an alkyl group. SELECTED DRAWING: None COPYRIGHT: (C)2019,JPOandINPIT

Synthesis and photochemical properties of aluminum, gallium, silicon, and tin naphthalocyanines

Ford, William E.,Rodgers, Michael A. J.,Schechtman, Lee A.,Sounik, James R.,Rihter, Boris D.,Kenney, Malcolm E.

, p. 3371 - 3377 (2008/10/08)

The synthesis and characterization of 30 Al, Ga, Si, and Sn naphthalocyanines relevant to the search for improved photodynamic therapy agents are reported. The compounds that have been studied are AlNcCl, AlNcOH, AlNcOSi-(n-C6H13)3, (AlNcF)n, GaNcCl, GaNcOH, GaNcOH·2H2O, GaNcOSin-C6H13)3, (GaNcF)n, SiNc(O-n-C8H17)2, SiNc[(OCH2CH2)~17OCH3] 2, SiNc[(OCH2CH2)~43OCH3] 2, SiNc[4-OCH2CH2)~26OC6H 4C(CH3)2CH2C(CH3) 3]2, SiNc[4-OC6H4CO(OCH2CH2) 3OCH3]2, SiNc[OSi(n-C4H9)2(n-C18H 37)]2, SiNc[OSi(i-C4H9)2(n-C18H 37)]2, SiNc[OSi(CH3)2(CH2)10COOCH 3]2, SiNc(2/3-Cl)4Cl2, SiNc(2/3-Cl)4(O-n-C8H17)2, SiNc(2/3-Cl)4[OSi(n-C6H13)3] 2, SiNc[2/3-Cl)4(OH)2, SiNc(2/3-Br)4Cl2, SiNc(2/3-Br)4(O-n-C8H17)2, SiNc(2/3-Br)4[OSi(n-C6H13)3] 2, SiNc(2/3-Br)4(OH)2, SnNcCl2, SnNc, SnNcI2, SnNc(OH)2, and SnNc[OSi(n-C6H13)3]2. For nine of these compounds and for an additional compound, SiNc[OSi(n-C6H13)3]2, one or more of the following photoproperties have been determined: λQ, the Q(0,0)-band absorption maximum; ΦT, the triplet-state quantum yield or ΦT′, an approximation of ΦT; Δ∈T the triplet-minus-ground-state extinction coefficient difference at 590 nm; τT, the triplet-state lifetime in the absence of O2; and kox, the bimolecular rate constant for the quenching of the triplet state by O2. The values obtained show that λQ is essentially independent of the kinds of atoms in the 2 and 3 positions of the macrocycle and that ΦT is moderately and directly dependent on the atomic numbers of the atoms in the center and the 2 and 3 positions of the ring. In the case of the silicon naphthalocyanines, they show in addition that λQ, ΦT′, and τT are moderately dependent on the type of axial ligand present.

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