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2'-phenylethyl β-D-glucopyranosiduronic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18997-55-2

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18997-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18997-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,9 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18997-55:
(7*1)+(6*8)+(5*9)+(4*9)+(3*7)+(2*5)+(1*5)=172
172 % 10 = 2
So 18997-55-2 is a valid CAS Registry Number.

18997-55-2Downstream Products

18997-55-2Relevant academic research and scientific papers

Compounds for a controlled release of active molecules

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Page/Page column 9, (2017/02/28)

The present invention relates to the field of perfumery. More particularly, it concerns compounds comprising at least one β-glucuronide moiety capable of liberating a perfuming alcohol. The present invention concerns also the use of said compounds in perfumery as well as the perfuming compositions or perfumed articles, in particular deodorants or antiperspirants comprising the invention's compounds.

Experimental and kinetic studies of the Escherichia coli glucuronylsynthase: An engineered enzyme for the synthesis of glucuronide conjugates

Wilkinson, Shane M.,Watson, Morgan A.,Willis, Anthony C.,McLeod, Malcolm D.

supporting information; experimental part, p. 1992 - 2000 (2011/06/19)

The detection and study of glucuronide metabolites is essential in many fields including pharmaceutical development, sports drug testing, and the detection of agricultural residues. Therefore, the development of improved methods for the synthesis of glucuronide conjugates is an important aim. The glycosynthase derived from E. coli β-glucuronidase provides an efficient, scalable, single-step synthesis of β-glucuronides under mild conditions. In this article we report on experimental and kinetic studies of the E. coli glucuronylsynthase, including the influence of acceptor substrate, pH, temperature, cosolvents, and detergents, leading to optimized conditions for glucuronide synthesis. Enzyme kinetics also reveals that both substrate and product inhibition may occur in glucuronylsynthase reactions but that these effects can be ameliorated through the judicious choice of acceptor and donor substrate concentrations. An investigation of temporary polar substituents was conducted leading to improved aqueous solubility of hydrophobic steroidal acceptors. In this way the synthesis of the steroidal metabolite dehydroepiandrosterone 3-β-d-glucuronide was achieved in three steps and 86% overall yield from dehydroepiandrosterone.

Escherichia coli glucuronylsynthase: An engineered enzyme for the synthesis of β-glucuronides

Wilkinson, Shane M.,Liew, Chu W.,Mackay, Joel P.,Salleh, Hamzah M.,Withers, Stephen G.,McLeod, Malcolm D.

supporting information; experimental part, p. 1585 - 1588 (2009/04/10)

The glycosynthase derived from E. coli β-glucuronidase catalyzes the glucuronylation of a range of primary, secondary, and aryl alcohols with moderate to excellent yields. The procedure provides an efficient, stereoselective, and scalable single-step synthesis of β-glucuronides under mild conditions.

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