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2-amino-4-n-butylchlorobenzene is an organic compound with the chemical formula C10H14ClN. It is a derivative of chlorobenzene, featuring an amino group (-NH2) at the 2nd position and a butyl group (-C4H9) at the 4th position. 2-amino-4-n-butylchlorobenzene is characterized by its potential reactivity due to the presence of the amino and chloro groups, which can participate in various chemical reactions, such as nucleophilic substitution or electrophilic aromatic substitution. It is often used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. The compound's properties, such as its boiling point, melting point, and solubility, can be influenced by the presence of these functional groups, making it a versatile building block in organic synthesis.

2000-95-5

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2000-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2000-95-5 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 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2000-95:
(6*2)+(5*0)+(4*0)+(3*0)+(2*9)+(1*5)=35
35 % 10 = 5
So 2000-95-5 is a valid CAS Registry Number.

2000-95-5Relevant academic research and scientific papers

Substituted (2-Phenoxyphenyl)acetic Acids with Antiinflammatory Activity. 1

Atkinson, David C.,Godfrey, Keith E.,Meek, Bernard,Saville, John F.,Stillings, Michael R.

, p. 1353 - 1360 (2007/10/02)

The synthesis and antiinflammatory activity of a series of substituted (2-phenoxyphenyl)acetic acids are described.Initial screening in the adjuvant arthritis test showed that halogen substitution in the phenoxy ring enhanced activity considerably.Ulcerogenic potential, as measured by the minimum ulcerogenic dose (MUD), was low in almost all the acids tested. acetic acid possessed the most favorable combination of potency with low toxicity, including ulcerogenicity, and this compound is now in therapeutic use.

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