Home Cart Sign in  
Chemical Structure| 22854-00-8 Chemical Structure| 22854-00-8

Structure of 22854-00-8

Chemical Structure| 22854-00-8

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 22854-00-8 ]

CAS No. :22854-00-8
Formula : C8H13NO5
M.W : 203.19
SMILES Code : O[C@H]1[C@H](O)[C@@]2([H])N=C(C)O[C@@]2([H])O[C@@H]1CO

Safety of [ 22854-00-8 ]

Application In Synthesis of [ 22854-00-8 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 22854-00-8 ]

[ 22854-00-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3321-03-7 ]
  • [ 22854-00-8 ]
  • 2-{2-[5-hydroxy-2-methyl-4-(1,2,3,4-tetrahydroxybutyl)-4,5-dihydroimidazol-1-yl]acetylamino}-3-phenylpropionic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
72% In aq. phosphate buffer; water; at 30℃; for 24h;pH 9.0; 323.0 mg (1.59 mmol) of the GNO obtained in Synthesis Example 2 was dissolved in 0.2 M sodium phosphate buffer solution (pH 9.0) (9.0 mL)GlyPhe (88.9 mg, 400 mumol) dissolved in distilled water was added and the mixture was allowed to stand at 30 C. for 24 hours.The obtained reaction solution was subjected to reverse phase HPLC, and under the same conditions as (1) to (5) in Example 2,After separation and purification, it was lyophilized to give a colorless solid product (243.8 mg). From the above measurement results, it was confirmed that the obtained product was GN-GlyPhe (GlcNAcGlyPhe form) represented by the following structural formula (q), and the yield was 72%.
68% In aq. phosphate buffer; at 30℃; for 24h;pH 9.0; General procedure: 143.8 mg (702 mumol) of sugar oxazoline II was dissolved in 4.4 mL of 0.1 M sodium phosphate buffer (pH 9.0). To this was added a 247 muL (2.12 mumol) of pentylamine and the mixture was kept at 30 C for 24 hours. The reaction mixture was subjected to reverse-phase HPLC with an Inertsil ODS-3 column (10 x 250 mm) equilibrated with 100 mM ammonium acetate buffer (pH 7.0) at 40 C. After injection of a sample, the proportion of acetonitrile was increased with a linear gradient from 0% to 2% in 10 min and from 2% to 62% in 30 min at a flow rate of 4.8 ml/min. After lyophilization, 124.0 mg (60%) of III was obtained as a mixture with NH4OAc.
 

Historical Records