• Nicotinamide riboside chloride

Nicotinamide riboside chloride

  • CasNo:23111-00-4
  • Purity:99%

Product Details;

CasNo: 23111-00-4

Molecular Formula: C11H15ClN2O5

Chinese Good Producer Factory direct supply Nicotinamide riboside chloride 23111-00-4 Fast Shipping

  • Molecular Formula:C11H15N2O5.Cl
  • Molecular Weight:290.703
  • PSA:116.89000 
  • LogP:-4.61120 

23111-00-4 Relevant articles

New crystalline salts of nicotinamide riboside as food additives

Haase, Robert,Hery-Barranco, Adrian,Pala, Laura,Parris, Jaclyn,Schabert, Günter,Spingler, Bernhard,Spitz, Urs

, (2021)

NR+ is a highly effective vitamin B3 typ...

Preparation method β - nicotinamide ribose chloride

-

Paragraph 0039; 0078; 0082-0098, (2021/11/10)

The invention belongs to the technical f...

Synthesis method of beta-nicotinamide riboside chloride

-

Paragraph 0017; 0024-0029, (2021/03/11)

The invention discloses a synthesis meth...

NMN intermediate NR chloride synthesis method

-

Paragraph 0045; 0051-0052, (2021/05/29)

The invention provides an intermediate s...

23111-00-4 Process route

5’,3‘,2’-tri-O-acetyl-1-β-D-ribofuranosylnicotinamide chloride
109527-15-3

5’,3‘,2’-tri-O-acetyl-1-β-D-ribofuranosylnicotinamide chloride

3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium (β-D-nicotinamide riboside)
23111-00-4

3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium (β-D-nicotinamide riboside)

Conditions
Conditions Yield
With ammonia; In methanol; at -3 ℃; for 24h; Temperature;
89.3%
With ammonia; In methanol; at -15 - -10 ℃; Temperature; Reagent/catalyst;
82%
With ethanol; ammonia; at 10 - 20 ℃; for 3h;
78%
With methanol; ammonia; at -5 - 0 ℃; for 12h; Large scale;
78%
With hydrogenchloride; In methanol; ethanol; at 20 ℃; for 4h;
64%
With ammonia; In methanol; at 0 ℃; for 14h; Large scale;
60%
With methanol; ammonia;
With hydrogenchloride; In methanol; for 12h; Reagent/catalyst; Solvent; Sealed tube;
With methanol; propylamine; at -5 ℃; for 22h; Temperature;
1-[(2R,3S,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofur-2-yl]-1,4-dihydropyridine-3-carboxamide
19132-12-8

1-[(2R,3S,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofur-2-yl]-1,4-dihydropyridine-3-carboxamide

3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium (β-D-nicotinamide riboside)
23111-00-4

3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium (β-D-nicotinamide riboside)

Conditions
Conditions Yield
With ammonium chloride; In water; at 20 ℃; for 1h; Solvent;
100%
With 5%-palladium/activated carbon; ammonium chloride; In isopropyl alcohol; at 20 ℃; for 20h; under 1500.15 Torr; Reagent/catalyst; Temperature; Solvent; Pressure; Green chemistry;
89%

23111-00-4 Upstream products

  • 109527-15-3
    109527-15-3

    5’,3‘,2’-tri-O-acetyl-1-β-D-ribofuranosylnicotinamide chloride

  • 122620-02-4
    122620-02-4

    3-carbamoyl-1-(tri-O-benzoyl-β-D-ribofuranosyl)-pyridinium; chloride

  • 6974-32-9
    6974-32-9

    1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose

  • 105499-44-3
    105499-44-3

    2,3,5-tri-O-acetyl-α-D-ribofuranosyl chloride

23111-00-4 Downstream products

  • 1094-61-7
    1094-61-7

    nicotinamide mononucleotide

  • 19132-12-8
    19132-12-8

    1-[(2R,3S,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofur-2-yl]-1,4-dihydropyridine-3-carboxamide

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