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1201-91-8

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1201-91-8 Usage

Uses

Different sources of media describe the Uses of 1201-91-8 differently. You can refer to the following data:
1. 4-[(2-hydroxyethyl)methylamino]-Benzaldehyde is used in the synthesis crosslinkable tricyanopyrroline polymeric electro-optic materials. 4-[(2-hydroxyethyl)methylamino]-Benzaldehyde is also used in th e chemical process when synthesizing polymethacrylates.
2. N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde may be used to synthesize:2,5-bis[4-(methylaminoethanol)benzylidene]cyclopentanone4′-[(2-tosyloxyethyl)(methyl)amino]-4-phenyl-3-buten-2-malonitrile, a tosylate precursormethanesulfonic acid 2-[(4-formyl-phenyl)-methyl-amino]-ethyl ester

Check Digit Verification of cas no

The CAS Registry Mumber 1201-91-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1201-91:
(6*1)+(5*2)+(4*0)+(3*1)+(2*9)+(1*1)=38
38 % 10 = 8
So 1201-91-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2/c1-11(6-7-12)10-4-2-9(8-13)3-5-10/h2-5,8,12H,6-7H2,1H3

1201-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-((2-Hydroxyethyl)(methyl)amino)benzaldehyde

1.2 Other means of identification

Product number -
Other names N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde

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:1201-91-8 SDS

1201-91-8Relevant articles and documents

Versatile near-infrared fluorescent probe for in vivo detection of Aβ oligomers

Li, Xiaofang,Li, Yuyan,Peng, Kewen,Ran, Chongzhao,Xu, Yungen,Yang, Jian,Zeng, Fantian

, (2020)

Amyloid-β oligomers (AβOs) enrichment in brain is highly related to Alzheimer's pathogenesis, but tracing them in the brain by imaging technique is still a great challenge due to their heterogeneity and metastability. Herein, a new near-infrared (NIR) fluorescent probe, namely, PTO-41, was designed and synthesized to specifically target AβOs. PTO-41 possesses excellent functional properties including optimal fluorescent properties (emission maxima at 680 nm upon interacting with AβOs), high affinity (Kd = 349 nM), low cell toxicity, desirable lipophilicity (log P = 2.24), and fast wash out from the brain (brain2 min/brain60 min = 5.0). Furthermore, PTO-41 exhibits a high sensitivity toward AβOs in vitro phantom imaging experiments. More importantly, PTO-41 shows great capacity to differentiate between 4-month-old APP/PS1 model mice from age-matched control mice using in vivo imaging. In summary, PTO-41 almost meets all the requirements as a versatile NIR fluorescent probe for the detection of AβOs both in vitro and in vivo.

A Multiaddressable Dyad with Switchable Cyan/Magenta/Yellow Colors for Full-Color Rewritable Paper

Qin, Tianyou,Han, Jiaqi,Geng, Yue,Ju, Le,Sheng, Lan,Zhang, Sean Xiao-An

supporting information, p. 12539 - 12545 (2018/09/10)

Reversible multicolor displays on solid media created from single-molecule pigments are a long-awaited goal. Herein, a new and simple molecular dyad, which can undergo switchable cyan (C), magenta (M), and yellow (Y) color changes in both solution and the solid state upon exposure to light, water/acid, and nucleophiles, has been designed and synthesized. The stimuli used herein can be applied independent of each other, which is beneficial for color changes without mutual interference. For comparison, mixtures of the two molecular switching motifs that form the basis of the dyad were also studied. The dyad greatly outperforms the corresponding mixed system with respect to reversible color switching on the paper substrate. Its potential for full-color rewritable paper with excellent reversibility has been demonstrated. Legible multicolor prints, that is, high color contrast and resolution, good dispersion, and excellent reversibility, were achieved by using common water-jet and light-based printers. This work provides a very promising approach for the further development of full-color switchable molecules, materials, and displays.

Mitochondria two-photon fluorescence viscosity probe and preparation method thereof

-

Paragraph 0048-0049, (2017/08/28)

The invention discloses a mitochondria two-photon fluorescence viscosity probe and a preparation method thereof. The structural formula of the mitochondria two-photon fluorescence viscosity probe is defined in the description. A target molecule has the go

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