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6-Amino-1,3-dimethyl-5-phenylazouracil is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54014-80-1

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54014-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54014-80-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,1 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54014-80:
(7*5)+(6*4)+(5*0)+(4*1)+(3*4)+(2*8)+(1*0)=91
91 % 10 = 1
So 54014-80-1 is a valid CAS Registry Number.

54014-80-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-imino-1,3-dimethyl-5-(phenylhydrazinylidene)-1,3-diazinane-2,4-dione

1.2 Other means of identification

Product number -
Other names 2,4(1H,3H)-Pyrimidinedione,6-amino-1,3-dimethyl-5-(phenylazo)

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:54014-80-1 SDS

54014-80-1Relevant academic research and scientific papers

A straight forward and first total synthesis of Penilumamides B–D

Reddy Penjarla, Thirupathi,Kundarapu, Maheshwar,Syed Mohd., Baquer,Bhattacharya, Anupam

, p. 3347 - 3349 (2017/08/02)

A simple and straight forward first total synthesis of rare lumazine peptides, Penilumamide B, C and D isolated from the marine-derived fungi Aspergillus and Penicillium sp. is described from a common starting material, 1,3-dimethyllumazine-6-carboxylic acid. Penilumamide C was prepared from Penilumamide B by oxidation of the methionine residue to the corresponding sulphone.

Synthesis, structure and study of azo-hydrazone tautomeric equilibrium of 1,3-dimethyl-5-(arylazo)-6-amino-uracil derivatives

Debnath, Diptanu,Roy, Subhadip,Li, Bing-Han,Lin, Chia-Her,Misra, Tarun Kumar

, p. 185 - 197 (2015/01/30)

Azo dyes, 1,3-dimethyl-5-(arylazo)-6-aminouracil (aryl = -C6H5 (1), -p-CH3C6H4 (2), -p-ClC6H4 (3), -p-NO2C6H4 (4)) were prepared and characterized by UV-vis, FT-IR, 1H NMR, 13C NMR spectroscopic techniques and single crystal X-ray crystallographic analysis. In the light of spectroscopic analysis it evidences that of the tautomeric forms, the azo-enamine-keto (A) form is the predominant form in the solid state whereas in different solvents it is the hydrazone-imine-keto (B) form. The study also reveals that the hydrazone-imine-keto (B) form exists in an equilibrium mixture with its anionic form in various organic solvents. The solvatochromic and photophysical properties of the dyes in various solvents with different hydrogen bonding parameter were investigated. The dyes exhibit positive solvatochromic property on moving from polar protic to polar aprotic solvents. They are fluorescent active molecules and exhibit high intense fluorescent peak in some solvents like DMSO and DMF. It has been demonstrated that the anionic form of the hydrazone-imine form is responsible for the high intense fluorescent peak. In addition, the acid-base equilibrium in between neutral and anionic form of hydrazone-imine form in buffer solution of varying pH was investigated and evaluated the pKa values of the dyes by making the use of UV-vis spectroscopic methods. The determined acid dissociation constant (pKa) values increase according to the sequence of 2 > 1 > 3 > 4.

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