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N1-BENZYL-4-NITRO-1,2-BENZENEDIAMINE, also known as benzyl-4-nitro-1,2-phenylenediamine, is a nitro aromatic amine with the molecular formula C13H12N4O2. It is a yellow crystalline powder that is insoluble in water but soluble in organic solvents. This chemical compound is primarily used as an intermediate in the synthesis of dyes, pigments, and other organic compounds. Due to its potential toxicological effects, it is classified as an irritant and sensitizer, and appropriate caution should be exercised during its handling and use.

66108-86-9

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66108-86-9 Usage

Uses

Used in Chemical Synthesis Industry:
N1-BENZYL-4-NITRO-1,2-BENZENEDIAMINE is used as a chemical intermediate for the synthesis of dyes and pigments, contributing to the production of various colorants used in different applications.
Used in Organic Compounds Synthesis:
N1-BENZYL-4-NITRO-1,2-BENZENEDIAMINE is used as a precursor in the synthesis of other organic compounds, playing a crucial role in the creation of a wide range of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 66108-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,0 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66108-86:
(7*6)+(6*6)+(5*1)+(4*0)+(3*8)+(2*8)+(1*6)=129
129 % 10 = 9
So 66108-86-9 is a valid CAS Registry Number.

66108-86-9Relevant academic research and scientific papers

2-(4-ARYL-1H-IMIDAZOL-1-YL)ANILINE COMPOUNDS

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Paragraph 0080, (2015/11/27)

The present invention provides compounds that are useful as vaccine adjuvants and/or antitumor agents and methods for producing and using the same. In one particular aspect of the invention, compounds of the invention are of the formula (I) where R1, R2, R3 and Ar1 are those defined herein.

Metal-free TEMPO-promoted C(sp3)-H amination to afford multisubstituted benzimidazoles

Xue, Ding,Long, Ya-Qiu

, p. 4727 - 4734 (2014/06/09)

An efficient TEMPO-air/cat. TEMPO-O2 oxidative protocol was developed to synthesize multisubstituted or fused tetracyclic benzimidazoles via a metal-free oxidative C-N coupling between the sp3 C-H and free N-H of readily available N1-benzyl/alkyl-1,2-phenylenediamines.

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