51714-09-1

Basic information

• Product Name: RAC 3-ACETAMIDO-NONAN-2-ONE
• Synonyms: RAC 3-ACETAMIDO-NONAN-2-ONE;3-AcetaMidononan-2-one;N-(1-Acetylheptyl)acetaMide;NSC 272452
• CAS NO: 51714-09-1
• Molecular Formula: C11H21NO2
• Molecular Weight: 199.28994
• Product Categories: All Aliphatics;Aliphatics;Intermediates
• Mol File: 51714-09-1.mol
• Article Data: 4

Chemical Properties

• Melting Point: 45-47°C
• Boiling Point: 344.2°C at 760 mmHg
• Flash Point: 131.8°C
• Appearance: /
• Density: 0.933g/cm³
• Vapor Pressure: 6.69E-05mmHg at 25°C
• Refractive Index: 1.443
• Storage Temp.: -20°C Freezer
• Solubility: Chloroform, DMSO, Ethyl Acetate
• CAS DataBase Reference: RAC 3-ACETAMIDO-NONAN-2-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: RAC 3-ACETAMIDO-NONAN-2-ONE(51714-09-1)
• EPA Substance Registry System: RAC 3-ACETAMIDO-NONAN-2-ONE(51714-09-1)

Safety Data

• Hazardous Substances Data: 51714-09-1(Hazardous Substances Data)

Usage

Chemical Properties

Yellow Solid

Uses

Intermediate in the production of adenosine deaminase inhibitors

InChI:InChI=1/C11H21NO2/c1-4-5-6-7-8-11(9(2)13)12-10(3)14/h11H,4-8H2,1-3H3,(H,12,14)

Upstream product

• 22433-33-6 Nona-1,2-dien 
• 75-05-8 acetonitrile 
• 644-90-6 2-aminooctanoic acid 

Relevant articles and documents

Stem Cell Culture Methods

The invention provides methods for reversibly inhibiting stem cell differentiation wherein a compound of formula (I) is contacted with a stem cell. The invention further provides a method for preparing a culture medium, a culture medium supplement and a composition comprising a compound of formula (I).

Method of imparting immunomodulating and antiviral activity

Compounds of the formula STR1 where X is OH, NH2, SH, OR or SR (where R is alkyl of 1 to 4 carbon atoms or benzyl), R1 is H or alkyl of 1 to 8 carbon atoms, R2 is H or methyl, Y is the salt of an amine of the formula STR2 where R3 and R4 are lower alkyl, e.g., 1 to 4 carbon atoms and n is an integer of 2 to 4 with p-acetamidobenzoic acid and where z is a number from 0 to 10 are useful as immunomodulators, as antiviral agents and in specific cases have anti-leukemic activity. The compounds and compositions where z is 1 to 10 are novel per se. When R2 is H the presence of Y enhances the immunoregulatory activity and the antiviral activity. If X is the NH2 there is immunoinhibitory activity but no immunostimulatory (immunopotentiatory) activity.