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1159408-54-4

  • Product Name:5-[(3,4,6-Tri-O-acetyl-2-acetylamido-2-deoxy-b-D-galactopyranosyl)oxy]pentanoic acid
  • Molecular Formula:
  • Purity:99%
  • Molecular Weight:447.439
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Product Details;

CasNo: 1159408-54-4

Reasoble Price High Quality For Sale 5-[(3,4,6-Tri-O-acetyl-2-acetylamido-2-deoxy-b-D-galactopyranosyl)oxy]pentanoic acid 1159408-54-4

  • Molecular Formula:C19H29NO11
  • Molecular Weight:447.439

1159408-54-4 Relevant articles

Multivalent N -acetylgalactosamine-conjugated siRNA localizes in hepatocytes and elicits robust RNAi-mediated gene silencing

Nair, Jayaprakash K.,Willoughby, Jennifer L. S.,Chan, Amy,Charisse, Klaus,Alam, Md. Rowshon,Wang, Qianfan,Hoekstra, Menno,Kandasamy, Pachamuthu,Kelin, Alexander V.,Milstein, Stuart,Taneja, Nate,Oshea, Jonathan,Shaikh, Sarfraz,Zhang, Ligang,Van Der Sluis, Ronald J.,Jung, Michael E.,Akinc, Akin,Hutabarat, Renta,Kuchimanchi, Satya,Fitzgerald, Kevin,Zimmermann, Tracy,Van Berkel, Theo J. C.,Maier, Martin A.,Rajeev, Kallanthottathil G.,Manoharan, Muthiah

, p. 16958 - 16961 (2014)

Conjugation of small interfering RNA (si...

OLIGONUCLEOTIDES CONTAINING NUCLEOTIDE ANALOGS

-

Page/Page column 237; 240; 241, (2021/03/13)

The present disclosure relates to double...

TARGETED PLASMA PROTEIN DEGRADATION

-

Page/Page column 172-175, (2021/08/14)

The present invention is directed to the...

S-ANTIGEN TRANSPORT INHIBITING OLIGONUCLEOTIDE POLYMERS AND METHODS

-

Paragraph 0068; 0470, (2021/06/22)

Various embodiments provide STOPS? polym...

LIGAND-2'-MODIFIED NUCLEIC ACIDS, SYNTHESIS THEREOF AND INTERMEDIATE COMPOUNDS THEREOF

-

, (2021/03/05)

The present invention relates to methods...

1159408-54-4 Process route

4-benzyloxycarbonylbutyl-2-deoxy-2-N-acetyl-3,4,6-tri-O-acetyl-β-D-galactopyranoside

4-benzyloxycarbonylbutyl-2-deoxy-2-N-acetyl-3,4,6-tri-O-acetyl-β-D-galactopyranoside

5-(((2R,3R,4R,5R,6R)-3-acetamido-4,5-diacetoxy-6-(acetoxymethyl)tetrahydro-2H-pyran-2-yl)oxy)pentanoic acid
1159408-54-4

5-(((2R,3R,4R,5R,6R)-3-acetamido-4,5-diacetoxy-6-(acetoxymethyl)tetrahydro-2H-pyran-2-yl)oxy)pentanoic acid

Conditions
Conditions Yield
With palladium 10% on activated carbon; hydrogen; In methanol; ethyl acetate;
98%
With palladium 10% on activated carbon; hydrogen; In methanol; at 15 ℃; under 775.743 Torr;
97%
With hydrogen; palladium; In methanol;
95%
With hydrogen; palladium; In methanol;
95%
With hydrogen; palladium; In methanol;
95%
With hydrogen; palladium; In methanol;
95%
With hydrogen; palladium; In methanol;
95%
With palladium 10% on activated carbon; hydrogen; In methanol;
95%
With palladium 10% on activated carbon; hydrogen; In methanol; ethyl acetate; at 20 ℃;
95.5%
With 5%-palladium/activated carbon; hydrogen; In methanol; at 20 ℃; for 18h; under 2482.38 Torr;
84%
With hydrogen; palladium; In methanol;
82%
With palladium 10% on activated carbon; hydrogen; In ethyl acetate; at 25 ℃; for 3h;
82%
With palladium 10% on activated carbon; In ethanol; cyclohexene; for 6h; Inert atmosphere; Reflux;
70%
With palladium 10% on activated carbon; In ethanol; cyclohexane; for 6h; Inert atmosphere; Reflux;
70%
With palladium 10% on activated carbon; In ethanol; cyclohexane; for 6h; Inert atmosphere; Reflux;
70%
With palladium 10% on activated carbon; cyclohexene; In ethanol; for 6h; Inert atmosphere; Reflux;
70%
With palladium 10% on activated carbon; hydrogen; In methanol; ethyl acetate;
hex-5'-enyl 3,4,6-tri-O-acetyl-2-acetylamino-2-deoxy-β-D-glucoside
210765-64-3

hex-5'-enyl 3,4,6-tri-O-acetyl-2-acetylamino-2-deoxy-β-D-glucoside

GlucNAc acid
1159408-54-4

GlucNAc acid

Conditions
Conditions Yield
With ruthenium trichloride; sodium periodate; In dichloromethane; acetonitrile; at 20 ℃; for 2.5h;
69.31%
hex-5'-enyl 3,4,6-tri-O-acetyl-2-acetylamino-2-deoxy-β-D-glucoside; With sodium periodate; In dichloromethane; water; acetonitrile; at 10 ℃; for 0.25h;
With ruthenium trichloride; In dichloromethane; water; acetonitrile; for 2.5h;
65%

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