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3-(3-nitrophenylamino)propanenitrile is an organic compound with the molecular formula C9H8N2O2. It is a derivative of benzene, featuring a nitro group (-NO2) attached to the phenyl ring at the meta position (3rd position). The molecule also contains an amino group (-NH2) bonded to the phenyl ring, and a propenenitrile group (-CH2CH=CH-CN) attached to the nitrogen atom. 3-(3-nitrophenylamino)propanenitrile is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of dyes and pigments. Due to its reactive nature, it is important to handle this chemical with care, following proper safety protocols.

2008-99-3

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2008-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2008-99-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,0 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2008-99:
(6*2)+(5*0)+(4*0)+(3*8)+(2*9)+(1*9)=63
63 % 10 = 3
So 2008-99-3 is a valid CAS Registry Number.

2008-99-3Downstream Products

2008-99-3Relevant academic research and scientific papers

An effective aza-michael addition of aromatic amines to electron-deficient alkenes in alkaline Al2O3

Ai, Xin,Wang, Xin,Liu, Jin-Ming,Ge, Ze-Mei,Cheng, Tie-Ming,Li, Run-Tao

, p. 5373 - 5377 (2010)

Aza-Michael addition of aromatic or aliphatic amines with various electron-deficient alkenes was performed using alkaline Al2O 3 as solid media at room temperature afforded the corresponding Michael addition products in good to excellent yields.The alkaline Al 2O3 can be easily recovered and reused.

Functionalized ionic liquid promoted aza-michael addition of aromatic amines

Liu, Xiao-Bing,Lu, Ming,Lu, Ting-Ting,Gu, Guo-Liang

experimental part, p. 1221 - 1226 (2011/10/02)

A functionalized ionic liquid, 3-(N,N-dimethyldodecylammonium) propanesulfonic acid hydrogen sulphate ([DDPA][HSO4]) has been used as catalyst for the aza-Michael reactions of aromatic amines with α,β-unsaturated compounds at room temperature to produce β-amino compounds in good yields. The catalyst can be reused for several times without obvious loss of the catalytic activity.

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