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2-Formyl-benzoesaeure-tosylhydrazon, also known as 2-formylbenzoic acid tosylhydrazone, is an organic compound with the chemical formula C14H13N2O4S. It is a derivative of 2-formylbenzoic acid, where the aldehyde group is protected by a tosylhydrazone moiety. 2-Formyl-benzoesaeure-tosylhydrazon is used as a protecting group in organic synthesis, particularly for aldehydes, to prevent unwanted side reactions during complex chemical transformations. The tosylhydrazone group can be selectively removed under mild conditions, allowing the aldehyde to be regenerated when needed. This makes 2-formyl-benzoesaeure-tosylhydrazon a valuable tool in the synthesis of complex organic molecules, such as pharmaceuticals and natural products.

6383-60-4

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6383-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6383-60-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,8 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6383-60:
(6*6)+(5*3)+(4*8)+(3*3)+(2*6)+(1*0)=104
104 % 10 = 4
So 6383-60-4 is a valid CAS Registry Number.

6383-60-4Relevant academic research and scientific papers

N-Tosylhydrazine-mediated deoxygenative hydrogenation of aldehydes and ketones catalyzed by Pd/C

Zhou, Lei,Liu, Zhenxing,Liu, Yizhou,Zhang, Yan,Wang, Jianbo

, p. 6083 - 6087 (2013)

A mild and efficient method for the deoxygenative hydrogenation of aldehydes and ketones has been developed. The reaction is mediated by N-tosylhydrazine with H2 (1 atm) as the reductant and 10% Pd/C as the catalyst.

Straightforward reductive esterification of carbonyl compounds with carboxylic acids through tosylhydrazone intermediates

Garcia-Munoz, Angel-Humberto,Tomas-Gamasa, Maria,Perez-Aguilar, M. Carmen,Cuevas-Yanez, Erick,Valdes, Carlos

scheme or table, p. 3925 - 3928 (2012/08/28)

The reaction of carboxylic acids with tosylhydrazones in basic media gives rise to the corresponding esters through an O-H insertion reaction in the in situ generated diazo compound. The process is operationally very simple, catalyst free, and very general with regard to the structure of both coupling partners. In particular, the esterification can be accomplished by employing tosylhydrazones derived from enolizable carbonyl compounds. Considering the ready availability of tosylhydrazones from carbonyl compounds, this reaction can be visualized as a reductive esterification of carbonyl compounds.

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