30407-81-9 Usage
Uses
Used in Dye and Pigment Production:
1,8-Naphthalenediamine,N1-phenylis used as a key intermediate in the production of various dyes and pigments. Its unique chemical structure allows for the creation of a wide range of colors, making it valuable in the dye and pigment industry.
Used in Pharmaceutical Synthesis:
As an intermediate in the synthesis of pharmaceuticals, 1,8-Naphthalenediamine,N1-phenylplays a crucial role in the development of new drugs. Its chemical properties enable the formation of various organic compounds, contributing to the advancement of pharmaceutical research and drug discovery.
Used in Organic Compound Synthesis:
1,8-Naphthalenediamine,N1-phenylis also utilized as an intermediate in the synthesis of various organic compounds. Its versatility in chemical reactions allows for the creation of a broad spectrum of organic molecules, which can be applied in different industries, such as chemical manufacturing and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 30407-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,4,0 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30407-81:
(7*3)+(6*0)+(5*4)+(4*0)+(3*7)+(2*8)+(1*1)=79
79 % 10 = 9
So 30407-81-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H14N2/c17-14-10-4-6-12-7-5-11-15(16(12)14)18-13-8-2-1-3-9-13/h1-11,18H,17H2
30407-81-9Relevant academic research and scientific papers
PYRIMIDINE-BASED COMPOUND AND ORGANIC LIGHT EMITTING DEVICE USING THE SAME
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Paragraph 0119-0122, (2016/10/08)
The present invention relates to a pyrimidine-based compound and an organic light emitting device including the same. According to an embodiment of the present invention, the pyrimidine-based compound can be used to form an organic layer in the organic light emitting device.COPYRIGHT KIPO 2015
1,8-Bis(diphenylamino)- and 1,8-Bis(methylphenylamino)naphthalene: Molecular Structure and Dynamic Behavior
Rimmler, Goesta,Krieger, Claus,Neugebauer, Franz A.
, p. 723 - 728 (2007/10/02)
The title compounds 2 and 3 have been synthesized from 1,8-diaminonaphthalene.The molecular structure of 2 has been determined by X-ray structure analysis and is discussed with regard to the arrangement of the peri-diphenylamino substituents in the crysta
HETEROCYCLIC ANALOGS OF PLEIADIENE. 55. 2-AZIDOPERIMIDINES: STABILITY OF THE TETRAZOLE FORM
Konstantinchenko, A. A.,Lyashenko, P. I.,Pozharskii, A. F.
, p. 832 - 835 (2007/10/02)
2-Azidoperimidine and its 1-methyl, 1-benzyl, and 1-phenyl derivatives were synthesized by the action of sodium azide on the corresponding 2-chloroperimidines.The IR spectra constitute evidence for the existence of all of these compounds in both the solid
