Home Halogens (3R,5S)-rel-5-[6-(2,4-Dichlorophenyl)hexyl]tetrahydro-3-hydroxy-2-oxo-3-furanaceticacid

(3R,5S)-rel-5-[6-(2,4-Dichlorophenyl)hexyl]tetrahydro-3-hydroxy-2-oxo-3-furanaceticacid

CAS No.:
154566-12-8
Catalog Number:
AG01ENNA
Molecular Formula:
C18H22Cl2O5
Molecular Weight:
389.2703
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1mg
≥95%
1 week
United States
$119
- +
5mg
99%
1 week
United States
$216
- +
10mg
99%
1 week
United States
$335
- +
50mg
99%
1 week
United States
$1050
- +
100mg
99%
1 week
United States
$1779
- +
Product Description
Catalog Number:
AG01ENNA
Chemical Name:
(3R,5S)-rel-5-[6-(2,4-Dichlorophenyl)hexyl]tetrahydro-3-hydroxy-2-oxo-3-furanaceticacid
CAS Number:
154566-12-8
Molecular Formula:
C18H22Cl2O5
Molecular Weight:
389.2703
MDL Number:
MFCD28127018
IUPAC Name:
2-[(3S,5R)-5-[6-(2,4-dichlorophenyl)hexyl]-3-hydroxy-2-oxooxolan-3-yl]acetic acid
InChI:
InChI=1S/C18H22Cl2O5/c19-13-8-7-12(15(20)9-13)5-3-1-2-4-6-14-10-18(24,11-16(21)22)17(23)25-14/h7-9,14,24H,1-6,10-11H2,(H,21,22)/t14-,18+/m1/s1
InChI Key:
YTRNLFYTHYWDAU-KDOFPFPSSA-N
SMILES:
OC(=O)C[C@@]1(O)C[C@H](OC1=O)CCCCCCc1ccc(cc1Cl)Cl
Properties
Complexity:
472  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Defined Bond Stereocenter Count:
0
Exact Mass:
388.084g/mol
Formal Charge:
0
Heavy Atom Count:
25  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
389.269g/mol
Monoisotopic Mass:
388.084g/mol
Rotatable Bond Count:
9  
Topological Polar Surface Area:
83.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
5.1  
Literature
Title Journal
Highly efficient and concise synthesis of both antipodes of SB204900, clausenamide, neoclausenamide, homoclausenamide and zeta-clausenamide. Implication of biosynthetic pathways of Clausena alkaloids. Organic & biomolecular chemistry 20090621
The biology and chemistry of hyperlipidemia. Bioorganic & medicinal chemistry 20070715
ATP citrate lyase inhibition can suppress tumor cell growth. Cancer cell 20051001
The role of adenosine triphosphate citrate lyase in the metabolism of acetyl coenzyme a and function of blood platelets in diabetes mellitus. Metabolism: clinical and experimental 20040101
Properties