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1-p-tolylsulfonylamino-8-nitronaphthalene is a complex organic chemical compound characterized by a naphthalene core, which is a fused ring system consisting of two benzene rings. The molecule features a nitro group (-NO2) at the 8-position, which is known for its strong electron-withdrawing properties and can impart explosive or reactive characteristics to the compound. Additionally, it has a p-tolylsulfonylamino group (-NHSO2C6H4-CH3-p) attached at the 1-position, where the p-tolyl refers to a toluene (methyl-phenyl) group located at the para position relative to the sulfonyl group (-SO2-). 1-p-tolylsulfonylamino-8-nitronaphthalene is likely used in advanced chemical research or as an intermediate in the synthesis of more complex molecules, given its highly functionalized nature. Due to the presence of both nitro and sulfonyl groups, it may exhibit unique reactivity patterns and could be of interest in the fields of materials science or pharmaceuticals.

76874-30-1

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76874-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76874-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,7 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76874-30:
(7*7)+(6*6)+(5*8)+(4*7)+(3*4)+(2*3)+(1*0)=171
171 % 10 = 1
So 76874-30-1 is a valid CAS Registry Number.

76874-30-1Relevant academic research and scientific papers

PERI-NAPHTHYLENEDIAMINES. 1. ?-DONOR CHARACTERISTICS OF 1,8-NAPHTHYLENEDIAMINES AND 2,3-DIHYDROPERIMIDINES

Pozharskii, A. F.,Suslov, A. N.,Starshikov, N. M.,Popova, L. L.,Klyuev, N. A.,Adanin, V. A.

, p. 1890 - 1901 (2007/10/02)

The ionization constants,IR and UV spectra, ionization potentials, and the tendency to form ? complexes with 1,3,5-trinitrobenzene were investigated in the series of N-methylated 1,8-naphthylenediamines and 2,3-dihydroperimidines.In spite of the distortion of the planar structure in 1,8-bis(dimethylamino)naphthalene, the conjugation of the dimethylamino groups with the naphthalene ring is extremely significant.The synthesis of 1-amino-8-methylaminonaphthalene and 1-amino-8-dimethylaminonaphthalene is described.

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