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7-(4-nitro-phenylcarbamoyl)-heptanoic acid is a complex organic compound with the molecular formula C14H16N2O5. It is characterized by a heptanoic acid backbone, which is a seven-carbon chain with a carboxylic acid group at one end. The key feature of 7-(4-nitro-phenylcarbamoyl)-heptanoic acid is the 4-nitro-phenylcarbamoyl group attached to the seventh carbon of the heptanoic acid chain. This group consists of a nitro group (-NO2) attached to a phenyl ring, which is in turn connected to an amide group (-CO-NH-) that binds to the heptanoic acid. The presence of the nitro group and the amide linkage gives 7-(4-nitro-phenylcarbamoyl)-heptanoic acid unique chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research.

5502-67-0

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5502-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5502-67-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,0 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5502-67:
(6*5)+(5*5)+(4*0)+(3*2)+(2*6)+(1*7)=80
80 % 10 = 0
So 5502-67-0 is a valid CAS Registry Number.

5502-67-0Relevant academic research and scientific papers

Racemization free longer N-terminal peptide hydroxamate synthesis on solid support using ethyl 2-(tert-butoxycarbonyloxyimino)-2-cyanoacetate

Manne, Srinivasa Rao,Thalluri, Kishore,Giri, Rajat Subhra,Paul, Ashim,Mandal, Bhubaneswar

supporting information, p. 6108 - 6111 (2015/10/28)

A facile, efficient, racemization-free, and environment friendly protocol for the synthesis of peptide hydroxamic acids directly from carboxylic/amino acids by ethyl 2-(tert-butoxycarbonyloxyimino)-2-cyanoacetate in the presence of DIPEA/DMAP at room temperature is described. The compatibility of this method with Fmoc based solid phase peptide synthesis (SPPS) is also demonstrated by synthesizing three relatively large N-terminal peptide hydroxamic acids on resin. Also, some biologically important hydroxamates are synthesized using this protocol.

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