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1H-Azepine-1-carboxylic acid, 2,3,4,7-tetrahydro-3,4-bis(phenylmethoxy)-2-[(phenylmethoxy)methyl]-, phenylmethyl ester, (2R,3R,4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

724705-48-0

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  • NewblueCHEM-1H-Azepine-1-carboxylic acid, 2,3,4,7-tetrahydro-3,4-bis(phenylmethoxy)-2-[(phenylmethoxy)methyl]-, phenylmethyl ester, (2R,3R,4R)-

    Cas No: 724705-48-0

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724705-48-0 Usage

Azepine ring

A seven-membered nitrogen-containing ring structure.

Carboxylic acid

A functional group with a carboxyl (-COOH) group.

Phenylmethoxy groups

Two methoxy (-OCH3) groups attached to a phenyl ring.

Ester functional group

A carbonyl group (C=O) with an oxygen atom on each side bonded to different organic groups.

Stereochemistry

The compound has a (2R,3R,4R)designation, indicating the specific three-dimensional arrangement of the molecule's atoms.

Potential applications

The compound may have a wide range of potential applications in the fields of pharmaceuticals, organic synthesis, and materials science, but further research is necessary to determine its exact properties and uses.

Check Digit Verification of cas no

The CAS Registry Mumber 724705-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,4,7,0 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 724705-48:
(8*7)+(7*2)+(6*4)+(5*7)+(4*0)+(3*5)+(2*4)+(1*8)=160
160 % 10 = 0
So 724705-48-0 is a valid CAS Registry Number.

724705-48-0Relevant articles and documents

Synthesis of d -Fagomine and Its Seven- and Eight-Membered Higher-Ring Analogues, and the Formal Synthesis of (+)-Australine from l -Xylose-Derived Chiron

Das, Pintu,Ajay, Sama,Shaw, Arun K.

, p. 3753 - 3762 (2016/11/08)

The synthesis of d-fagomine and its seven- and eight-membered higher-ring analogues from commercially available l-xylose is reported. The syntheses involve elaboration of a common alkenol precursor obtained from l-xylose-derived hemiacetal. The key steps

The first synthesis of substituted azepanes mimicking monosaccharides: A new class of potent glycosidase inhibitors

Li, Hongqing,Bleriot, Yves,Chantereau, Caroline,Mallet, Jean-Maurice,Sollogoub, Matthieu,Zhang, Yongmin,Rodriguez-Garcia, Eliazar,Vogel, Pierre,Jimenez-Barbero, Jesus,Sinay, Pierre

, p. 1492 - 1499 (2007/10/03)

The synthesis of the first examples of seven-membered ring iminoalditols, molecules displaying an extra hydroxymethyl substituent on their seven-membered ring compared to the previously reported polyhydroxylated azepanes, has been achieved from D-arabinos

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