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2,2':6',2''-Terpyridine, 4'-[4-(1,1-dimethylethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

157557-32-9

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157557-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157557-32-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,5,5 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 157557-32:
(8*1)+(7*5)+(6*7)+(5*5)+(4*5)+(3*7)+(2*3)+(1*2)=159
159 % 10 = 9
So 157557-32-9 is a valid CAS Registry Number.

157557-32-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-tert-butylphenyl)-2,6-dipyridin-2-ylpyridine

1.2 Other means of identification

Product number -
Other names 2,2':6',2''-Terpyridine,4'-[4-(1,1-dimethylethyl)phenyl]

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:157557-32-9 SDS

157557-32-9Relevant academic research and scientific papers

Non-innocence of 1,4-dicyanamidobenzene bridging ligands in dinuclear ruthenium complexes.

Choudhuri, Mohommad M. R.,Kaim, Wolfgang,Sarkar, Biprajit,Crutchley, Robert J.

, p. 11060 - 11066 (2013)

Four dinuclear complexes, [{RuII(ttpy)(bpy)}2(μ-L) ][PF6]2, where bpy is 2,2′-bipyridine, ttpy is 4-(tert-butylphenyl)-2,2′:6′,2″-terpyridine, and L is 2,5-dimethyl-, 2,5-dichloro-, 2,3,4,5-tetrachloro- and unsu

Near-infrared fluorescent ruthenium complex and application thereof in tumor photocatalytic drugs

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Paragraph 0046; 0053-0055, (2021/08/06)

The invention relates to the technical field of medicines, in particular to a near-infrared fluorescent ruthenium complex and application thereof in tumor photocatalytic drugs. The invention discloses a near-infrared fluorescent ruthenium complex, which has near-infrared fluorescence, has a relatively strong curative effect of photodynamic therapy on cervical cancer (HeLa cells) compared with the absorption peak red shift of most of the existing ruthenium complexes in a visible light region, has IC50 as low as 0.029 [mu]M under the condition of illumination, has a very strong growth inhibition capability on human cervical cancer cell strains, and has a photodynamic therapy index (PI) as high as 353.931. The complex can generate singlet oxygen under an illumination condition, and has a photocatalytic oxidation effect on NADH and NADPH at the same time. The complex has important significance for researching high-efficiency novel anti-tumor drugs, can be used for further preparing anti-tumor drugs, and has relatively high application value.

Use of metal complex compounds as catalysts for oxidation using molecular oxygen or air

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Page/Page column 18, (2010/02/15)

Use, as a catalyst for oxidation reactions using molecular oxygen and/or air, of at least one metal complex compound of formula (1) wherein Me is manganese, titanium, iron, cobalt, nickel or copper, X is a coordinating or bridging radical, n and m are each independently of the other an integer having a value of from 1 to 8, p is an integer having a value of from 0 to 32, z is the charge of the metal complex, Y is a counter-ion, q=z/(charge of Y), and L is a ligand of formula (2) wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10 and R11 are each independently of the others hydrogen; unsubstituted or substituted C1-C18alkyl or aryl; cyano; halogen; nitro; —COOR12 or —SO3R12 wherein R12 is in each case hydrogen, a cation or unsubstituted or substituted C1-C18alkyl or aryl; —SR13, —SO2R13 or —OR13 wherein R13 is in each case hydrogen or unsubstituted or substituted C1-C18alkyl or aryl; —NR14R15; —(C1-C6alkylene)-NR14R15; —N(+)R14R15R16; —(C1-C6alkylene)-N(+)R14R15R16; —N(R13)—(C1-C6alkylene)-NR14R15; —N[(C1-C6alkylene)-NR14R15]2; —N(R13)—(C1-C6alkylene)-N(+)R14R15R16; —N[(C1-C6alkylene)-N(+)R14R15R16]2; —N(R13)—N—R14R15 or —N(R13)N″R14R15R16, wherein R13 is as defined above and R14, R15 and R16 are each independently of the other(s) hydrogen or unsubstituted or substituted C1-C18alkyl or aryl, or R14 and R15, together with the nitrogen atom linking them, form an unsubstituted or substituted 5-, 6- or 7-membered ring which may contain further hetero atoms. [in-line-formulae][LnMemXp]zYq??(1) [/in-line-formulae]

4-tert-butylphenyl solubilized oligopyridines

Constable, Edwin C.,Harverson, Peter,Smith, Diane R.,Whall, Louise A.

, p. 7799 - 7806 (2007/10/02)

Soluble 4-tert-butylphenyl substituted derivatives of 2,2':6',2''-terpyridine, 2,2':6',2'':6'',2'''-quaterpyridine, 2,2':6',2'':6'',2''':6''',2''''-quinquepyridine and 2,2':6',2'':6'',2''':6''',2'''':6'''',2'''''-sexipyridine have been prepared. The ligan

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