α-D-Mannose Pentaacetate

Basic information

  • Product Name:α-D-Mannose Pentaacetate
  • CasNo.:4163-65-9
  • MF:C16H22O11
  • MW:390.344

Physical and Chemical Properties

  • Boiling Point:64-75 °C
  • Packing:customer require
  • Throughput:
Inquiry

Product Details

CasNo: 4163-65-9

MF: C16H22O11

Packing: customer require

Quality Factory Sells Top Purity 99% α-D-Mannose Pentaacetate 4163-65-9 with Safe Delivery

 

Synonyms: Penta-O-acetyl-alpha-D-mannopyranose; 1,2,3,4,6-Penta-O-acetyl-alpha-D-mannose; alpha-D-Mannopyranose pentaacetate; D-alpha-Mannose pentaacetate; 1,2,3,4,6-penta-O-acetyl-alpha-D-mannopyranose; D-Mannose Pentacetate; α-D-mannose pentaacetate; 1,2,3,4,6-Penta-O-acetyl-D-Mannopyranose.

Molecular Formula: C16H22O11

Molecular Weight: 390.34

CAS Number: 4163-65-9

Item Specification
Appearance White to off-white crystalline powder
Assay(GC), % ≥98.0
Melting point, °C 64.0~75.0
Specific rotation , 

 (C=1,CHCl3)

+51.0~+57.0
Water,% ≤1.0
Residue on ignition, % ≤0.10

Characteristics: The product is a White to off-white crystalline powder. It is readily soluble in CHCl3 and insoluble in water.

1,2,3,4,6-PENTA-O-ACETYL-ALPHA-D-MANNOPYRANOSE(Cas 4163-65-9) Usage

This product can be used to synthesis the mannose-conjugated (trans-R,R-cyclohexane-1,2-diamine)-2-flouromalonato-platinum(II) complex which shows  cytotoxicity to MCF-7 cell line, mannose-cationic conjugated polymers, photodynamic therapy agents such as amphiphilic glycosylated lipid porphyrin, photoluminescent functionalized silicon nanocrystals bearing D-mannose for cancer cells imaging, polymeric drug delivery systems that containing mannose-based, the anti-inflammatory, analgesic activity of tocopherol, morphine and targeting of bleomycin are both increased when they contain mannopyranoyl- or conjugate carbamoylmannose moiety. It is also used to synthesis thioglycoside, N-glycoside of mannose and bromo-tetra-O-acetyl mannopyranose and so on.

Package: customer require.

Expiration Date: 2 years

4163-65-9 Relevant articles

PROCESS OF SYNTHESIS OF β-6'SULFOQUINOVOSYL DIACYLGLYCEROLS

-

Page/Page column 11; 12, (2022/02/28)

The present invention relates to a synth...

Selectivity of 1-O-Propargyl-D-Mannose Preparations

?ezanka, Michal,Dolensky, Bohumil,Krabicová, Ilona

, (2022/03/01)

Thanks to their ability to bind to speci...

Design, Synthesis, biological investigations and molecular interactions of triazole linked tacrine glycoconjugates as Acetylcholinesterase inhibitors with reduced hepatotoxicity

Ahmed, Ajaz,Bhagat, Kavita,Choudhary, Sushil,Kaur Gulati, Harmandeep,Kumar, Ajay,Kumar, Nitish,Mukherjee, Debaraj,Singh Bedi, Preet Mohinder,Singh, Atamjit,Singh, Harbinder,Vir Singh, Jatinder

, (2021/11/23)

Tacrine is a known Acetylcholinesterase ...

Synthesis and biological evaluation of 3β-O-neoglycosides of caudatin and its analogues as potential anticancer agents

Li, Xiao-San,Chen, Tang-Ji,Xu, Zhi-Peng,Long, Juan,He, Miao-Ying,Zhan, He-Hui,Zhuang, Hai-Cai,Wang, Qi-Lin,Liu, Li,Yang, Xue-Mei,Tang, Jin-Shan

, (2021/12/30)

In order to study the structure–activity...

4163-65-9 Process route

1-(4-hydroxy-3,5-dimethoxy-phenyl)-ethanone
2478-38-8

1-(4-hydroxy-3,5-dimethoxy-phenyl)-ethanone

acetic anhydride
108-24-7

acetic anhydride

2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide
572-09-8

2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide

D-glucose pentaacetate
83-87-4,604-68-2,604-69-3,2152-77-4,4026-35-1,4163-59-1,4163-60-4,4163-61-5,4163-65-9,4257-94-7,4257-96-9,16299-15-3,19186-39-1,19189-55-0,25878-60-8,25941-03-1,32445-48-0,32445-49-1,32445-53-7,32445-54-8,34685-58-0,34685-59-1,43168-42-9,43168-44-1,43169-22-8,43169-25-1,66966-07-2,70749-17-6,80184-01-6,93221-01-3,93221-02-4,99630-88-3,109215-53-4,115792-70-6,115792-73-9,139894-92-1,139973-25-4,144071-49-8,147648-81-5

D-glucose pentaacetate

1-(4-acetoxy-3,5-dimethoxy-phenyl)-ethanone
28294-47-5

1-(4-acetoxy-3,5-dimethoxy-phenyl)-ethanone

3,5-dimethoxy-4-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)acetophenone
86402-42-8

3,5-dimethoxy-4-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)acetophenone

Conditions
Conditions Yield
Yield given. Multistep reaction;
 
nudicauloside B

nudicauloside B

acetic anhydride
108-24-7

acetic anhydride

D-glucose pentaacetate
83-87-4,604-68-2,604-69-3,2152-77-4,4026-35-1,4163-59-1,4163-60-4,4163-61-5,4163-65-9,4257-94-7,4257-96-9,16299-15-3,19186-39-1,19189-55-0,25878-60-8,25941-03-1,32445-48-0,32445-49-1,32445-53-7,32445-54-8,34685-58-0,34685-59-1,43168-42-9,43168-44-1,43169-22-8,43169-25-1,66966-07-2,70749-17-6,80184-01-6,93221-01-3,93221-02-4,99630-88-3,109215-53-4,115792-70-6,115792-73-9,139894-92-1,139973-25-4,144071-49-8,147648-81-5

D-glucose pentaacetate

1,2,3,4-tetra-O-acetyl-L-arabinopyranose
1233-03-0,2595-11-1,4026-34-0,4049-33-6,4049-34-7,4257-95-8,4257-98-1,4258-00-8,4627-30-9,17080-99-8,19186-37-9,25227-11-6,25243-38-3,62446-93-9,62929-49-1,67226-03-3,78087-60-2,78088-17-2,82890-16-2,86782-34-5,86782-35-6,92218-63-8,99880-95-2,108646-05-5,115939-79-2,142130-89-0,123163-97-3

1,2,3,4-tetra-O-acetyl-L-arabinopyranose

Conditions
Conditions Yield
nudicauloside B; With hydrogenchloride; water; for 4h; Reflux;
With methyldioctylamine; In chloroform; water;
acetic anhydride; With pyridine; for 24h;
 

4163-65-9 Upstream products

  • 2280-44-6
    2280-44-6

    D-Glucose

  • 108-24-7
    108-24-7

    acetic anhydride

  • 57-50-1
    57-50-1

    Sucrose

  • 2478-38-8
    2478-38-8

    1-(4-hydroxy-3,5-dimethoxy-phenyl)-ethanone

4163-65-9 Downstream products

  • 13242-51-8
    13242-51-8

    1-O-p-nitrophenyl-2,3,4,6-tetra-O-acetyl α-D-mannopyranoside

  • 125354-48-5
    125354-48-5

    ethyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-mannopyranoside

  • 32934-24-0
    32934-24-0

    S-ethyl 2,3,4,6-tetra-O-acetyl-1-deoxy-1-thio-α-D-mannopyranoside

  • 37797-55-0
    37797-55-0

    1-O-phenyl-2,3,4,6-tetra-O-acetyl-β-D-mannopyranoside