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15871-95-1

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  • 4-Pyridinecarboxaldehyde,3-hydroxy-5-(hydroxymethyl)-2-methyl-,2-[[3-hydroxy-5-(hydroxymethyl)-2-methyl-4-pyridinyl]methylene]hydrazone

    Cas No: 15871-95-1

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  • 4-Pyridinecarboxaldehyde,3-hydroxy-5-(hydroxymethyl)-2-methyl-,2-[[3-hydroxy-5-(hydroxymethyl)-2-methyl-4-pyridinyl]methylene]hydrazone cas 15871-95-1

    Cas No: 15871-95-1

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15871-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15871-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,7 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15871-95:
(7*1)+(6*5)+(5*8)+(4*7)+(3*1)+(2*9)+(1*5)=131
131 % 10 = 1
So 15871-95-1 is a valid CAS Registry Number.

15871-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4Z)-5-(hydroxymethyl)-4-[[2-[(Z)-[5-(hydroxymethyl)-2-methyl-3-oxopyridin-4-ylidene]methyl]hydrazinyl]methylidene]-2-methylpyridin-3-one

1.2 Other means of identification

Product number -
Other names Pyridoxalazin

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:15871-95-1 SDS

15871-95-1Upstream product

15871-95-1Downstream Products

15871-95-1Relevant articles and documents

An aggregation-induced emission active vitamin B6cofactor derivative: Application in pH sensing and detection of latent fingerprints

Ashok Kumar, S. K.,Bhardwaj, Vinita,Crisponi, Guido,Sahoo, Suban K.,Thangaraj, Anand,Varddhan, Seshu

, p. 1402 - 1409 (2020/11/03)

Aggregation-induced emission (AIE) properties of an easy-to-prepare and structurally planar Schiff base derivative of the vitamin B6 cofactor pyridoxal (L) were investigated in DMSO-H2O mixed solvents. Compound L showed weak fluorescence (λem = 425 nm) in pure DMSO, but increasing the fraction of water in DMSO resulted in a significant fluorescence enhancement at 575 nm due to the restriction of intramolecular rotation (RIR) of L upon aggregation. SEM analyses revealed the formation of hairy micelle-like or needle-shaped self-assemblies/aggregates of L. The DFT calculations were performed to examine the tendency of L to form self-aggregates, and the results indicate the formation of several intramolecular non-covalent interactions that energetically favored the self-aggregation of L. The pH sensing study revealed that the red-emission of aggregates of L between pH 5.9 and 9.0 turned into green emission at the basic pH with the estimated pKa values of 9.39 and 10.22. Further, the aggregates of L were applied for the visualization of latent fingerprints (LFPs) over a non-porous glass slide.

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