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2-amino-4-n-butanoylchlorobenzene is an organic compound with the chemical formula C11H14ClNO. It is a derivative of chlorobenzene, featuring a chloro group attached to the benzene ring, an amino group at the 2-position, and a butanoyl group (a four-carbon acyl chain) at the 4-position. 2-amino-4-n-butanoylchlorobenzene is a potential intermediate in the synthesis of various pharmaceuticals and agrochemicals, as well as a precursor for the production of dyes and pigments. Due to its reactivity, it is important to handle 2-amino-4-n-butanoylchlorobenzene with care, as it can undergo further chemical reactions, such as nucleophilic substitution or addition reactions, depending on the specific conditions and reagents used.

2001-00-5

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2001-00-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2001-00-5 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 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2001-00:
(6*2)+(5*0)+(4*0)+(3*1)+(2*0)+(1*0)=15
15 % 10 = 5
So 2001-00-5 is a valid CAS Registry Number.

2001-00-5Relevant 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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