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5-aminohexane-1,2,3,4,6-pentol

Basic Information

  • CAS No.: 2351-14-6
  • Purity: 99%
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Details

Manufacturer Sells Best Quality 5-aminohexane-1,2,3,4,6-pentol 2351-14-6 with stock

  • Molecular Formula: C6H15NO5
  • Molecular Weight: 181.189
  • Vapor Pressure: 1.78E-13mmHg at 25°C 
  • Boiling Point: 530.7°C at 760 mmHg 
  • PKA: 11.66±0.45(Predicted) 
  • Flash Point: 274.7°C 
  • PSA: 127.17000 
  • Density: 1.506g/cm3 
  • LogP: -2.91870 

5-aminohexane-1,2,3,4,6-pentol(Cas 2351-14-6) Usage

General Description

5-aminohexane-1,2,3,4,6-pentol is a chemical compound with the molecular formula C6H15NO5. It is also known as D-lyxo-hexulose-1-amino-5-phosphate. 5-aminohexane-1,2,3,4,6-pentol is a sugar alcohol that contains an amino group. It is commonly used in biotechnology and pharmaceutical research as a starting material for the synthesis of various compounds, including potential drugs and bioactive molecules. 5-aminohexane-1,2,3,4,6-pentol has also shown potential as a chelating agent for metal ions and as an antioxidant, making it of interest for various industrial and medical applications. Additionally, this compound has been investigated for its potential role in the treatment of neurological disorders and metabolic diseases due to its ability to cross the blood-brain barrier and its effects on cellular metabolism.

InChI:InChI=1/C6H15NO5/c7-3(1-8)5(11)6(12)4(10)2-9/h3-6,8-12H,1-2,7H2

2351-14-6 Relevant articles

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Karrer,Meyer

, p. 626 (1937)

-

Purification and characterization of D-glucosaminitol dehydrogenase from Agrobacterium radiobacter.

Iwamoto,Sakamoto,Tamura,Mikata,Tanaka

, p. 785 - 791 (1999)

D-Glucosaminitol dehydrogenase, which ca...

Aminopolyols from Carbohydrates: Amination of Sugars and Sugar-Derived Tetrahydrofurans with Transaminases

Subrizi, Fabiana,Benhamou, Laure,Ward, John M.,Sheppard, Tom D.,Hailes, Helen C.

supporting information, p. 3854 - 3858 (2019/02/20)

Carbohydrates are the major component of...

Medium-chain dehydrogenases with new specificity: Amino mannitol dehydrogenases on the azasugar biosynthetic pathway

Wu, Yanbin,Arciola, Jeffrey,Horenstein, Nicole

, p. 10 - 14 (2014/01/17)

Azasugar biosynthesis involves a key deh...

Synthesis and PLA2-inhibitory properties of 2(R)-acetamido-alkylphosphomethanols with a variable aggregate anchor.

Kley,von Kiedrowski,Unger,Massing

, p. 261 - 264 (2007/10/03)

Acylamino inhibitors of 14 kDa-PLA2 were...

2351-14-6 Process route

2-amino-2-deoxyglucose
3416-24-8

2-amino-2-deoxyglucose

water
7732-18-5

water

2-amino-2-deoxy-D-glucitol
14307-03-0,2351-14-6

2-amino-2-deoxy-D-glucitol

D-glucosaminic acid
3646-68-2

D-glucosaminic acid

Conditions
Conditions Yield
Geschwindigkeit bei Raumtemperatur;
2-amino-2-deoxyglucose
3416-24-8

2-amino-2-deoxyglucose

water
7732-18-5

water

furan-2,3,5(4H)-trione pyridine (1:1)

furan-2,3,5(4H)-trione pyridine (1:1)

2-amino-2-deoxy-D-glucitol
14307-03-0,2351-14-6

2-amino-2-deoxy-D-glucitol

D-glucosaminic acid
3646-68-2

D-glucosaminic acid

Conditions
Conditions Yield
Geschwindigkeit bei Raumtemperatur;

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