Methyl 4,6-O-Benzylidene-α-D-Galactopyranoside

Basic information

  • Product Name:Methyl 4,6-O-Benzylidene-α-D-Galactopyranoside
  • CasNo.:72904-85-9
  • MF:C14H18 O6
  • MW:282.293

Physical and Chemical Properties

  • Purity:≥98.0
  • Boiling Point:
  • Packing:
  • Throughput:
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Product Details

CasNo: 72904-85-9

MF: C14H18 O6

Appearance: White to off-white crystalline powder

Purity: ≥98.0

Good factory supply good Methyl 4,6-O-Benzylidene-α-D-Galactopyranoside 72904-85-9

NAME:Methyl 4,6-O-benzylidene-α-D-galactopyranoside

CAS No.:72904-85-9

Quality Standard:

Item Specification
Appearance White to off-white crystalline powder  
Assay , %  ≥98.0 
Melting point, ℃ 168.0-175.0
Loss on drying, % ≤1.0 
Residue on ignition, % ≤0.10 
 

Methyl 4,6-O-benzylidene-α-D-galactopyranoside(Cas 72904-85-9) Usage

Methyl-4, 6-benzylidene -α -D-galactopyranoside is a commonly used benzylidene protected carbohydrate derivative, usually as an intermediate, widely used in the synthesis of a variety of compounds.

72904-85-9 Relevant articles

Acceleration and deceleration factors on the hydrolysis reaction of 4,6-O-benzylidene acetal group

Maki, Yuta,Kajihara, Yasuhiro,Nomura, Kota,Okamoto, Ryo,Izumi, Masayuki,Mizutani, Yasuhisa

, p. 15849 - 15856 (2021/01/18)

The benzylidene acetal group is one of t...

Exploration of the Fluoride Reactivity of Aryltrifluoroborate on Selective Cleavage of Diphenylmethylsilyl Groups

Fujiki, Katsumasa,Tanaka, Katsunori

supporting information, p. 4616 - 4620 (2020/07/06)

The first known report on the fluoride c...

Binding of the Bacterial Adhesin FimH to Its Natural, Multivalent High-Mannose Type Glycan Targets

Sauer, Maximilian M.,Jakob, Roman P.,Luber, Thomas,Canonica, Fabia,Navarra, Giulio,Ernst, Beat,Unverzagt, Carlo,Maier, Timm,Glockshuber, Rudi

, p. 936 - 944 (2019/01/11)

Multivalent carbohydrate-lectin interact...

Conformational analysis of the disaccharide methyl a-d-mannopyranosyl-(1→3)-2-O-acetyl-β-D-manno-pyranoside monohydrate

Zhang, Wenhui,Wu, Qingquan,Oliver, Allen G.,Serianni, Anthony S.

, p. 610 - 615 (2019/06/14)

The crystal structure of methyl β-d-mann...

72904-85-9 Process route

benzaldehyde dimethyl acetal
1125-88-8

benzaldehyde dimethyl acetal

Methyl mannoside
22277-65-2

Methyl mannoside

Methyl-4,6-O-(phenylmethylene)-β-D-mannopyranoside
3162-96-7,4148-58-7,4153-17-7,4288-93-1,5328-47-2,6988-39-2,13566-32-0,14155-23-8,27994-50-9,37093-57-5,37093-59-7,57701-27-6,59168-66-0,64552-06-3,65391-13-1,65391-14-2,65530-26-9,66512-65-0,71117-36-7,71117-37-8,71117-41-4,72904-85-9,74560-56-8,79549-74-9,86783-81-5,96093-51-5,98633-13-7,110415-35-5,110415-36-6,110850-29-8,124020-29-7,126924-12-7,129263-21-4,131433-03-9,145920-49-6,146863-04-9

Methyl-4,6-O-(phenylmethylene)-β-D-mannopyranoside

Conditions
Conditions Yield
With toluene-4-sulfonic acid; In N,N-dimethyl-formamide; at 20 ℃; for 48h;
65%
With toluene-4-sulfonic acid; In N,N-dimethyl-formamide; at 20 ℃;
61%
benzaldehyde dimethyl acetal
1125-88-8

benzaldehyde dimethyl acetal

(2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol
617-04-9

(2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol

methyl-4,6-O-phenylmethylene-α-D-mannopyranoside
3162-96-7,4148-58-7,4153-17-7,4288-93-1,5328-47-2,6988-39-2,13566-32-0,14155-23-8,27994-50-9,37093-57-5,37093-59-7,57701-27-6,59168-66-0,64552-06-3,65391-13-1,65391-14-2,65530-26-9,66512-65-0,71117-36-7,71117-37-8,71117-41-4,72904-85-9,74560-56-8,79549-74-9,86783-81-5,96093-51-5,98633-13-7,110415-35-5,110415-36-6,110850-29-8,124020-29-7,126924-12-7,129263-21-4,131433-03-9,145920-49-6,146863-04-9

methyl-4,6-O-phenylmethylene-α-D-mannopyranoside

Conditions
Conditions Yield
With camphor-10-sulfonic acid;
98%
With 1,3,5-trichloro-2,4,6-triazine; In acetonitrile; at 60 ℃; for 0.166667h; regioselective reaction; Sonication; Inert atmosphere;
98%
With toluene-4-sulfonic acid; 1-butyl-3-methylimidazolium Tetrafluoroborate; at 80 ℃; for 2h;
88%
With 3,4-bis((3,5-bis(trifluoromethyl)phenyl)amino)cyclobut-3-ene-1,2-dione; In acetonitrile; at 20 ℃; for 2.5h; Inert atmosphere;
86%
With toluene-4-sulfonic acid; In N,N-dimethyl-formamide; at 50 - 70 ℃; for 4h;
78%
With toluene-4-sulfonic acid; In N,N-dimethyl-formamide; acetonitrile;
77%
With perchloric acid on silica gel; In N,N-dimethyl-formamide; at 20 ℃;
73%
With toluene-4-sulfonic acid; In N,N-dimethyl-formamide; at 60 ℃; for 1h; Inert atmosphere;
70%
With toluene-4-sulfonic acid; In N,N-dimethyl-formamide; at 60 ℃; for 1h;
70%
With toluene-4-sulfonic acid; In N,N-dimethyl-formamide; at 60 ℃; for 1h;
70%
With toluene-4-sulfonic acid; In N,N-dimethyl-formamide; at 60 ℃; for 2h; under 150.015 Torr;
52%
With camphor-10-sulfonic acid; In N,N-dimethyl-formamide; at 20 ℃; for 24h;
48%
With camphor-10-sulfonic acid; In N,N-dimethyl-formamide; at 60 ℃; for 32.75h; under 195.016 Torr;
37%
With toluene-4-sulfonic acid; In N,N-dimethyl-formamide; at 60 ℃; for 6h; under 150.015 Torr;
31%
With camphor-10-sulfonic acid; In N,N-dimethyl-formamide; at 20 ℃;
 
In N,N-dimethyl-formamide; at 40 ℃; for 4h;
12 g
With iodine; In acetonitrile; at 20 ℃; for 3h;
 

72904-85-9 Upstream products

  • 51223-62-2
    51223-62-2

    methyl β-D-galactopyranoside

  • 1125-88-8
    1125-88-8

    benzaldehyde dimethyl acetal

  • 617-04-9
    617-04-9

    (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol

  • 100-52-7
    100-52-7

    benzaldehyde

72904-85-9 Downstream products

  • 74984-87-5
    74984-87-5

    Methyl-4,5-O-benzyliden-2,3-carbonato-α-D-mannopyranosid

  • 120200-50-2
    120200-50-2

    methyl 4,6-O-benzylidene-2,3-di-O-methyl-α-D-mannopyranoside

  • 7177-79-9
    7177-79-9

    methyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

  • 98392-36-0
    98392-36-0

    Methyl 2-O-acetyl-4,6-O-(phenylmethylene)-α-D-mannopyranoside