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Benzenemethanol, 4-[(4-hydroxyphenyl)azo]-, also known as 4-(4-hydroxyphenylazo)benzenemethanol or 4-(4-hydroxyphenylazo)benzyl alcohol, is an organic compound with the chemical formula C13H12N2O2. It is a derivative of benzenemethanol, featuring an azo group (-N=N-) connecting a 4-hydroxyphenyl group to the benzyl alcohol moiety. This yellow crystalline solid is primarily used as a chemical intermediate in the synthesis of various azo dyes and pigments, which are widely employed in the textile, plastics, and printing industries. The compound is known for its stability, colorfastness, and solubility properties, making it a valuable component in the production of high-quality colorants.

91955-16-7

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91955-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91955-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,5 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91955-16:
(7*9)+(6*1)+(5*9)+(4*5)+(3*5)+(2*1)+(1*6)=157
157 % 10 = 7
So 91955-16-7 is a valid CAS Registry Number.

91955-16-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[[4-(hydroxymethyl)phenyl]hydrazinylidene]cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names Benzylalkohol<4azo4>phenol

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:91955-16-7 SDS

91955-16-7Relevant academic research and scientific papers

Hypoxia-Activated PEGylated Conditional Aptamer/Antibody for Cancer Imaging with Improved Specificity

Zhou, Fang,Fu, Ting,Huang, Qin,Kuai, Hailan,Mo, Liuting,Liu, Honglin,Wang, Qianqian,Peng, Yongbo,Han, Dongmei,Zhao, Zilong,Fang, Xiaohong,Tan, Weihong

, p. 18421 - 18427 (2019)

Aptamers and antibodies, as molecular recognition probes, play critical roles in cancer diagnosis and therapy. However, their recognition ability is based on target overexpression in disease cells, not target exclusivity, which can cause on-target off-tumor effects. To address the limitation, we herein report a novel strategy to develop a conditional aptamer conjugate which recognizes its cell surface target, but only after selective activation, as determined by characteristics of the disease microenvironment, which, in our model, involve tumor hypoxia. This conditional aptamer is the result of conjugating the aptamer with PEG5000-azobenzene-NHS, which is responsive to hypoxia, here acting as a caging moiety of conditional recognition. More specifically, the caging moiety is unresponsive in the intact conjugate and prevents target recognition. However, in the presence of sodium dithionite or hypoxia (2) or in the tumor microenvironment, the caging moiety responds by allowing conditional recognition of the cell-surface target, thereby reducing the chance of on-target off-tumor effects. It is also confirmed that the strategy can be used for developing a conditional antibody. Therefore, this study demonstrates an efficient strategy by which to develop aptamer/antibody-based diagnostic probes and therapeutic drugs for cancers with a unique hypoxic microenvironment.

Red light-triggered photoreduction on a nucleic acid template

Deussner-Helfmann, Nina,Duchstein, Patrick,Dutta, Subrata,Heilemann, Mike,Kn?r, Günther,Mokhir, Andriy,Rühle, Jennifer,Schikora, Margot,Zahn, Dirk,Zatsepin, Timofei

supporting information, p. 10026 - 10029 (2020/09/23)

Conjugate Sn(iv)(pyropheophorbide a)dichloride-(peptide nucleic acid) catalyzes reduction of azobenzene derivatives in the presence of complementary nucleic acid (NA) upon irridiation with red light (660 nm). This is the first red light-induced NA-templat

Hypoxia-Induced Pro-Protein Therapy Assisted by a Self-Catalyzed Nanozymogen

Li, Xudong,Wei, Yuansong,Wu, Yuchen,Yin, Lichen

supporting information, p. 22544 - 22553 (2020/10/12)

The success of intracellular protein therapy demands efficient delivery and selective protein activity in diseased cells. Therefore, a cascaded nanozymogen consisting of a hypoxia-activatable pro-protein, a hypoxia-inducing protein, and a hypoxia-strengthened intracellular protein delivery nanovehicle was developed. RPAB, an enzymatically inactive pro-protein of RNase, reversibly caged with hypoxia-cleavable azobenzene, was delivered with glucose oxidase (GOx) using hypoxia-responsive nanocomplexes (NCs) consisting of azobenzene-cross-linked oligoethylenimine (AOEI) and hyaluronic acid (HA). Upon NC-mediated delivery into cancer cells, GOx catalyzed glucose decomposition and aggravated tumoral hypoxia, which drove the recovery of RPAB back to the hydrolytically active RNase and expedited the degradation of AOEI to release more protein cargoes. Thus, the catalytic reaction of the nanozymogen was self-accelerated and self-cycled, ultimately leading to a cooperative anti-cancer effect between GOx-mediated starvation therapy and RNase-mediated pro-apoptotic therapy.

Light and reduction responsive supra-amphiphile for controllable fluorescence based on Pillar[6]arene

Wu, Yitao,Shangguan, Liqing,Liu, Peiren,Liu, Yuezhou,Li, Qi,Cao, Jiajun,Zhu, Huangtianzhi

, (2020/09/18)

As increasing demands of smart fluorescent materials, developing new systems with controllable emissions is more essential. Here we report a pillar[6]arene and tetraphenylethene (TPE)-based supra-amphiphile, which shows dual-responsiveness and tunable emi

Worm-like micelles can be formed of the light response type quaternary ammonium salt cationic surfactant and its synthetic method

-

Paragraph 0037; 0040; 0041, (2019/01/08)

The invention discloses a photo-responsive quaternary cationic surfactant capable of forming a wormlike micelle and a synthetic method thereof. The surfactant has a structural formula as shown in the specification. In the formula, R represents a straight-

Targeted dendrimer-drug conjugates

-

Page/Page column 45, (2016/06/13)

The invention provides for dendrimer conjugates useful for liver-specific delivery of therapeutic agents. The therapeutic agent is associated to the dendrimer through a enzyme-cleavable covalent linkage.

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