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Benzamide, N-(2-mercaptoethyl)-4-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73721-91-2

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73721-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73721-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,2 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73721-91:
(7*7)+(6*3)+(5*7)+(4*2)+(3*1)+(2*9)+(1*1)=132
132 % 10 = 2
So 73721-91-2 is a valid CAS Registry Number.

73721-91-2Upstream product

73721-91-2Downstream Products

73721-91-2Relevant academic research and scientific papers

Amine-boranes as Dual-Purpose Reagents for Direct Amidation of Carboxylic Acids

Choudhary, Shivani,Hamann, Henry J.,Ramachandran, P. Veeraraghavan

, (2020)

Amine-boranes serve as dual-purpose reagents for direct amidation, activating aliphatic and aromatic carboxylic acids and, subsequently, delivering amines to provide the corresponding amides in up to 99% yields. Delivery of gaseous or low-boiling amines as their borane complexes provides a major advantage over existing methodologies. Utilizing amine-boranes containing borane incompatible functionalities allows for the preparation of functionalized amides. An intermolecular mechanism proceeding through a triacyloxyborane-amine complex is proposed.

AMINE-BORANES AS BIFUNCTIONAL REAGENTS FOR DIRECT AMIDATION OF CARBOXYLIC ACIDS

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Paragraph 0008-0009; 0063-0064, (2022/03/04)

The present invention generally relates to a process for selective and direct activation and subsequent amidation of aliphatic and aromatic carboxylic acids to afford an amide R3CONR1R2. That the process is capable of delivering gaseous or low-boiling point amines provides a major advantage over existing methodologies, which involves an intermediate of triacyloxyborane-amine complex [(R3CO2)3—B—NHR1R2]. This procedure readily produces primary, secondary, and tertiary amides, and is compatible with the chirality of the acid and amine involved. The preparation of known pharmaceutical molecules and intermediates has also been demonstrated.

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