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O-benzoyl-N-p-toluoyl-hydroxylamine is a chemical compound with the molecular formula C14H13NO3. It is a derivative of hydroxylamine, featuring a benzoyl group attached to the oxygen atom and a p-toluoyl group attached to the nitrogen atom. O-benzoyl-N-p-toluoyl-hydroxylamine is often used as a reagent in organic synthesis, particularly in the preparation of various heterocyclic compounds and as a protecting group in peptide synthesis. It is known for its ability to react with aldehydes and ketones to form oximes, which can be further transformed into other useful compounds. The compound is typically synthesized through the reaction of hydroxylamine with benzoyl chloride and p-toluoyl chloride, and it is characterized by its melting point and spectral data. Due to its reactivity, it is important to handle O-benzoyl-N-p-toluoyl-hydroxylamine with care, following appropriate safety protocols.

6552-38-1

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6552-38-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6552-38-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6552-38:
(6*6)+(5*5)+(4*5)+(3*2)+(2*3)+(1*8)=101
101 % 10 = 1
So 6552-38-1 is a valid CAS Registry Number.

6552-38-1Downstream Products

6552-38-1Relevant academic research and scientific papers

Facile synthesis ofO-acylhydroxamatesviareaction of oxime chlorides with carboxylic acids

Chen, Rongxiang,Li, Yan-Li,Sun, Aili,Wang, Kai-Kai,Zhang, Shan-Shan,Zhao, Ying-Chao

, p. 40193 - 40196 (2021/12/31)

A simple and efficient method for the synthesis ofO-acylhydroxamate derivatives from oxime chlorides and carboxylic acids was developed. The reaction affords clean and facile access to diverseO-acylhydroxamates in high yields (up to 85%). The chemical structure of a typical product was confirmed using single-crystal X-ray structure analysis.

A very mild and selective method for O-benzoylation of hydroxamic acids

Zheng, Yongsheng,Liu, Muqiong,Yuan, Yu

supporting information, p. 4404 - 4406 (2014/07/22)

Selective O-benzoylation of hydroxamic acids is achieved by the treatment of BPO and DABCO. Aliphatic alcohols are not reactive under these conditions. Various radical or oxidation sensitive functional groups are compatible with this protocol, and no anhydrous reagents or solvents are required for the high yields of the benzoylations.

Regio-selective formation of O-acyl/O-benzoyl hydroxamates by using a polymer supported reagent strategy

Burungule,Bondge,Munde,Bhingolikar,Mane

, p. 1923 - 1927 (2007/10/03)

Rapid, quantitative and regioselective O-acylation/O-benzoylation of hydroxamic acids has been carried using polymer supported hydroxamate anions and acetyl/benzoyl chloride under mild conditions. The isolation of unambiguous and pure products by si-mple

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