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23222-97-1

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23222-97-1 Usage

Description

2-Nitro-p-xylylene Glycol is an organic compound with the molecular formula C8H8N2O5. It is a colorless crystalline solid and serves as an essential intermediate in the synthesis of various pharmaceutical compounds. Its chemical structure allows it to participate in multiple reactions, making it a versatile building block in the development of new drugs.

Uses

Used in Pharmaceutical Industry:
2-Nitro-p-xylylene Glycol is used as a reactant in the synthesis of furylsulfonamides, which are known as EP1 receptor antagonists. These antagonists play a crucial role in the treatment of various inflammatory diseases, such as arthritis, by blocking the action of prostaglandin E2 on the EP1 receptor, thereby reducing inflammation and pain.

Check Digit Verification of cas no

The CAS Registry Mumber 23222-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,2 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23222-97:
(7*2)+(6*3)+(5*2)+(4*2)+(3*2)+(2*9)+(1*7)=81
81 % 10 = 1
So 23222-97-1 is a valid CAS Registry Number.

23222-97-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(hydroxymethyl)-3-nitrophenyl]methanol

1.2 Other means of identification

Product number -
Other names 1,4-benzenedimethanol,2-nitro

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:23222-97-1 SDS

23222-97-1Downstream Products

23222-97-1Relevant articles and documents

18F-Labeled Benzyldiamine Derivatives as Novel Flexible Probes for Positron Emission Tomography of Cerebral β-Amyloid Plaques

Li, Zijing,Zhang, Xuran,Zhang, Xiaoyang,Cui, Mengchao,Lu, Jie,Pan, Xiaodong,Zhang, Xianzhong

, p. 10577 - 10585 (2016/12/16)

Early noninvasive visualization of cerebral β-amyloid (Aβ) plaques with positron emission tomography (PET) is the most feasible way to diagnose Alzheimer’s disease (AD). In this study, a series of flexible benzyldiamine derivatives (BDA) were proposed for

Photo-sensitive PMMA microgels: Light-triggered swelling and degradation

Klinger, Daniel,Landfester, Katharina

experimental part, p. 1426 - 1440 (2012/04/23)

Two classes (type A and type B) of novel photolabile divinyl functionalized crosslinkers based on o-nitrobenzyl derivatives were synthesized and investigated with regard to their photolytic performance upon UV irradiation. The systematic variation of the molecular structure resulted in different degradation rates depending on the irradiation conditions. Thus, the successive and independent cleavage is enabled by either adjusting the applied wavelengths or irradiation times. The respective molecules were used to build up photodegradable PMMA microgels by free radical copolymerization with MMA in a miniemulsion polymerization process. UV light-induced degradation of the swollen microgels was monitored by time dependent turbidity measurements and the resulting kinetics were found to correlate with the photolysis rates of the respective crosslinkers in solution. The irradiation wavelength-controlled selective partial cleavage of type B crosslinking points was achieved by UV irradiation with λ > 315 nm and resulted in particles with extensively increased volumes consisting of highly swollen networks. In addition, the irradiation time-controlled selective complete degradation of particles containing type B crosslinkers was accomplished. By using broadband UV light containing wavelengths of λ 315 nm, the successive complete particle disintegration of type B and type A microgels was observed. Hence, the specific performance of the synthesized microgels can be precisely triggered by means of the used UV light wavelengths, doses and intensities, thus representing a great potential as new light-responsive nanoscaled materials.

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