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52372-39-1

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52372-39-1 Usage

Flammability and Explosibility

Notclassified

Properties and Applications

TEST ITEMS SPECIFICATION APPEARANCE BRILLIANT RED POWDER SHADE BLUISH HEAT RESISTANCE 300 °C min LIGHT FASTNESS 7 ACID RESISTANCE 5 ALKALI RESISTANCE 5 WATER RESISTANCE 5 DENSITY 1.25 g/cm 3 RESIDUE ON 80 MESH 5.0% max WATER SOLUBLE 1.0% max VOLATITE 105 °C 1.0% max TINTING STRENGTH 100-105 %

TEST ITEMS

SPECIFICATION

APPEARANCE

BRILLIANT RED POWDER

SHADE

BLUISH

HEAT RESISTANCE

300 °C min

LIGHT FASTNESS

7

ACID RESISTANCE

5

ALKALI RESISTANCE

5

WATER RESISTANCE

5

DENSITY

1.25 g/cm 3

RESIDUE ON 80 MESH

5.0% max

WATER SOLUBLE

1.0% max

VOLATITE 105 °C

1.0% max

TINTING STRENGTH

100-105 %

Check Digit Verification of cas no

The CAS Registry Mumber 52372-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,7 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52372-39:
(7*5)+(6*2)+(5*3)+(4*7)+(3*2)+(2*3)+(1*9)=111
111 % 10 = 1
So 52372-39-1 is a valid CAS Registry Number.
InChI:InChI=1/C23H19N5O/c1-3-27(4-2)15-10-9-14-11-16-21(29-20(14)12-15)17(13-24)22(25)28-19-8-6-5-7-18(19)26-23(16)28/h5-12,25H,3-4H2,1-2H3/b25-22+

52372-39-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (7e)-3-(diethylamino)-7-imino-7h-chromeno[3',2':3,4]pyrido[1,2-a]benzimidazole-6-carbonitrile

1.2 Other means of identification

Product number -
Other names Solvent Red 197

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:52372-39-1 SDS

52372-39-1Relevant articles and documents

Construction of ratiometric hydrogen sulfide probe with two reaction sites and its applications in solution and in live cells

Fu, Deyang,Zhi,Lv,Luo, Yi,Xiong, Xiaoqing,Kang, Xiaohui,Hou, Wei,Yan, Jun,Zhao, Hongjuan,Zheng, Laijiu

, (2020)

Hydrogen sulfide (H2S), as the third multifunctional signaling biomolecule, it acts as a neuromodulator in the human brain and is recognized as an important gas transmitter in human physiology. The abnormal concentrations of H2S in human cells can result in several common diseases. Therefore, accurate, fast, and reliable methodologies are required for measuring the in vitro and in vivo concentrations of H2S to further investigate its function. In this study, a novel DR–SO2N3 fluorescent probe containing the fluorophore Disperse Red 277 and a sulfonyl azide group was developed and exploited based on the structural characteristic of Disperse Red 277 that contains the active site easily can be attacked by HS?. Therefore, this probe featured two reaction sites that involved the reduction and Michael addition of H2S and exhibited rapid ratiometric fluorescence changes and high selectivity towards H2S with a 619-fold enhancement factor. Further, the density functional theory (DFT)/time-dependent density functional theory (TDDFT) studies are conducted to understand the photophysical properties of DR–SO2N3 and the final product DRHS–SO2NH2, which makes the proposed mechanism more reasonable. Furthermore, the probe was successfully applied for the ratiometric fluorescence imaging of exogenous H2S in living cells.

Articles Comprising Benzopyran Colorants, Method Of Manufacture, And Method Of Use

-

Page/Page column 7, (2008/06/13)

An article comprising the compound of Formula (I) wherein X is hydrogen or a radical of Formula (II), R1 independently at each occurrence is a C1-C20 aliphatic radical, a C3-C10 cycloaliphatic radical, or a C3-C10 aromatic radical; R2, R3, R4 and R5 are independently at each occurrence a halogen, a nitro group, a cyano group, a hydroxy group, a C1-C20 aliphatic radical, a C3-C20 cycloaliphatic radical, or a C6-C20 aromatic radical; and “n”, “q”, and “p” are each independently integers having a value of 0 to 3, and “m” is an integer having a value of 0 to 4.

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