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13116-27-3

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13116-27-3 Usage

Chemical Properties

White to orange-brown crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 13116-27-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,1 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13116-27:
(7*1)+(6*3)+(5*1)+(4*1)+(3*6)+(2*2)+(1*7)=63
63 % 10 = 3
So 13116-27-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H7IN2/c7-5-1-3-6(9-8)4-2-5/h1-4,9H,8H2

13116-27-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L14806)  4-Iodophenylhydrazine, 95%   

  • 13116-27-3

  • 1g

  • 719.0CNY

  • Detail
  • Alfa Aesar

  • (L14806)  4-Iodophenylhydrazine, 95%   

  • 13116-27-3

  • 5g

  • 2846.0CNY

  • Detail
  • Aldrich

  • (638463)  4-Iodophenylhydrazine  95%

  • 13116-27-3

  • 638463-1G

  • 1,147.77CNY

  • Detail
  • Aldrich

  • (638463)  4-Iodophenylhydrazine  95%

  • 13116-27-3

  • 638463-5G

  • 4,378.14CNY

  • Detail

13116-27-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Iodophenylhydrazine

1.2 Other means of identification

Product number -
Other names (4-Iodophenyl)hydrazine

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:13116-27-3 SDS

13116-27-3Relevant articles and documents

Homo- and hetero-[3]rotaxanes with two π-systems clasped in a single macrocycle

Klotz, Eric J. F.,Claridge, Tim D. W.,Anderson, Harry L.

, p. 15374 - 15375 (2006)

Here we present the first synthesis of a [3]rotaxane with two dumbbell components threaded through a single γ-cyclodextrin macrocycle. This synthesis is carried out in two steps: first one dumbbell is synthesized threaded through the macrocycle to give a

Bistetrazine-Cyanines as Double-Clicking Fluorogenic Two-Point Binder or Crosslinker Probes

Kormos, Attila,Koehler, Christine,Fodor, Eszter A.,Rutkai, Zsófia R.,Martin, Madison E.,Mez?, Gábor,Lemke, Edward A.,Kele, Péter

, p. 8841 - 8847 (2018)

Fluorogenic probes can be used to minimize the background fluorescence of unreacted and nonspecifically adsorbed reagents. The preceding years have brought substantial developments in the design and synthesis of bioorthogonally applicable fluorogenic syst

Smart J-aggregate of cyanine photosensitizer with the ability to target tumor and enhance photodynamic therapy efficacy

Li, Miao,Sun, Wen,Tian, Ruisong,Cao, Jianfang,Tian, Ye,Gurram, Bhaskar,Fan, Jiangli,Peng, Xiaojun

, (2021)

Photodynamic therapy (PDT) has been demonstrated to be effective for cancer treatment. Design of photosensitizers (PS) featuring tumor targeting, long excitation wavelengths, and high singlet oxygen quantum yields (Φ(1O2)) is the cru

Studies on a vinyl ruthenium-modified squaraine dye: Multiple visible/near-infrared absorbance switching through dye- and substituent-based redox processes

Chen, Jing,Winter, Rainer F.

, p. 10733 - 10741 (2012)

The bis(vinyl ruthenium)-modified squaraine dye 1 was synthesized by treatment of [RuHCl(CO)(PiPr3)2] with bis(ethynyl)- substituted squaraine 8. Spectroscopic and electrochemical measurements on 1 and its organic precursors 6-8 were

Hypoxia-activated NIR photosensitizer anchoring in the mitochondria for photodynamic therapy

Xu, Feng,Li, Haidong,Yao, Qichao,Ge, Haoying,Fan, Jiangli,Sun, Wen,Wang, Jingyun,Peng, Xiaojun

, p. 10586 - 10594 (2019)

Photodynamic therapy is considered as a promising treatment for cancer, but still faces several challenges. The hypoxic environment in solid tumors, imprecise tumor recognition and the lack of selectivity between normal and cancer cells extremely hinder t

Iodinated xanthene-cyanine NIR dyes as potential photosensitizers for antimicrobial photodynamic therapy

Ebaston, T. M.,Gellerman, Gary,Nakonechny, Faina,Patsenker, Leonid,Talalai, Efrosiniia

, (2021)

Photosensitizers (PSs) are chemical entities that upon light exposure are able to produce cytotoxic species such as singlet oxygen superoxide and free radicals. PSs are used in photodynamic therapy applications (PDT) to eradicate cancer cells, pathogenic bacteria, fungi, and viruses. Development of the NIR-activatable photosensitizes with high phototoxicity and low toxicity in dark conditions is challenging. Here we first report on the synthesis and antimicrobial testing of the new NIR photosensitizers based on the iodinated xanthene-cyanine dyes. These new photosensitizers exhibit high antimicrobial efficacy on Staphylococcus aureus pathogens at low dye concentration (~0.5 μM) and low NIR light dose (24.3 J/cm2).

Photodynamic therapy with tumor cell discrimination through rna-targeting ability of photosensitizer

Jin, Xiaoyi,Li, Miao,Ma, Xiuqin,Tan, Yang,Tian, Ye,Xu, Yuan

supporting information, (2021/10/12)

Photodynamic therapy (PDT) represents an effective treatment to cure cancer. The targeting ability of the photosensitizer is of utmost importance. Photosensitizers that discriminate cancer cells can avoid the killing of normal cells and improve PDT effica

Bioorthogonally Applicable Fluorogenic Cyanine-Tetrazines for No-Wash Super-Resolution Imaging

Knorr, Gergely,Kozma, Eszter,Schaart, Judith M.,Németh, Krisztina,T?r?k, Gy?rgy,Kele, Péter

, p. 1312 - 1318 (2018/04/23)

The synthesis, fluorogenic characterization, and labeling application of four tetrazine-quenched cyanine probes with emission maxima in the red-far red range is reported. Fluorescence of the cyanine-cores is quenched via through-bond-energy-transfer (TBET) exerted by a bioorthogonal tetrazine unit. Upon bioorthogonal labeling reaction with cyclooctyne tagged proteins, the quenching effect ceases, and thus the fluorescence reinstates, resulting in an increase in fluorescence intensity. As a rare example among indocyanines, one of our new probes was found suitable in STED-based super-resolution imaging. The applicability of this fluorogenic Tet-Cy3 probe was therefore further demonstrated in the bioorthogonal labeling of cytoskeletal protein, actin, with subsequent super-resolution microscopy (STED) imaging even under no-wash conditions.

Iodinated cyanine dyes: a new class of sensitisers for use in NIR activated photodynamic therapy (PDT)

Atchison, Jordan,Kamila, Sukanta,Nesbitt, Heather,Logan, Kieran A.,Nicholas, Dean M,Fowley, Colin,Davis, James,Callan, Bridgeen,McHale, Anthony P,Callan, John F

supporting information, p. 2009 - 2012 (2017/02/15)

A new class of iodinated cyanine dyes have been prepared for use in NIR excited photodynamic therapy (PDT) and demonstrated improved efficacy in two pancreatic cell lines as well as excellent tumour control in a murine model of the disease.

MICROBUBBLE-CHEMOTHERAPEUTIC AGENT COMPLEX FOR SONODYNAMIC THERAPY

-

Page/Page column 54; 55, (2017/06/29)

The invention relates to methods of sonodynamic therapy comprising the co-administration of a microbubble-chemotherapeutic agent complex together with a microbubble-sonosensitiser complex. It further relates to pharmaceutical compositions comprising these

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