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β-Aspartamidinoacetic acid, also known as β-aspartyl-N-methylamide, is a synthetic compound derived from aspartic acid and methylamine. It is a dipeptide, consisting of two amino acids, aspartic acid and the methylated form of asparagine. β-aspartamidinoacetic acid is known for its potential use in the development of sweeteners, as it exhibits a sweet taste. It is also of interest in the field of pharmaceuticals and biochemistry due to its unique structure and potential applications in drug design. The compound is characterized by its ability to form stable salts and has been studied for its potential effects on metabolism and as a building block in the synthesis of more complex molecules.

72378-49-5

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72378-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72378-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,7 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72378-49:
(7*7)+(6*2)+(5*3)+(4*7)+(3*8)+(2*4)+(1*9)=145
145 % 10 = 5
So 72378-49-5 is a valid CAS Registry Number.

72378-49-5Downstream Products

72378-49-5Relevant academic research and scientific papers

A Quantitative Evaluation of Methods for Coupling Asparagine

Mojsov, Svetlana,Mitchell, Alexander R.,Merrifield, R. B.

, p. 555 - 560 (2007/10/02)

A quantitative procedure was developed to evaluate methods for coupling asparagine.Boc-asparagine was coupled to glycyloxymethylphenoxymethyl-copoly(styrene-divinylbenzene) resin under a variety of conditions, and the product, Asn-Gly, and any byproducts were cleaved from the resin with 50percent trifluoroacetic acid in methylene chloride.The mixture was then separated on a sulfonated ion exchange column and quantitated by the ninhydrin reaction.Coupling by the dicyclohexylcarbodiimide (DCC) or symmetrical anhydride methods gave large amounts of the dehydration product, β-cyanoalanylglycine, and smaller amounts of β-aspartamidinoacetic acid, α-aspartylglycine, and β-aspartylglycine in addition to the desired asparaginylglycine.Activation of Boc-Asn by DCC plus hydroxybenzotriazole or by the nitrophenyl ester gave 98 to 99percent of Asn-Gly, but very low levels of the byproducts were detectable with the sensitive chromatographic method.Protection of the amide function of Boc-Asn with the 4,4'-dimethoxybenzhydryl group avoided completely the formation of the nitrile during DCC coupling.Pure Ala(CN)-Gly was quantitatively reconverted to Asn-Gly by HF.The rehydration of nitrile also occurred in 50percent trifluoroacetic acid in dichloromethane, but much more slowly.

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