(-)-Corey Lactone Benzoate CAS 39746-00-4

Introduction:Basic information about (-)-Corey Lactone Benzoate CAS 39746-00-4, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

(-)-Corey Lactone Benzoate Basic information

Product Name:(-)-Corey Lactone Benzoate
Synonyms:5-(Benzoyloxy)hexahydro-4-(hydroxymethyl)-2H-cyclopenta[b]furan-2-one(3aα,4α,5β,6aα);(-)-5-(BENZOYLOXY)HEXAHYDRO-4-(HYDROXYME)-2H-CYCLOPENTA(B)FURAN-2-ONE, 97%;5-(BENZOYLOXY) HEXAHYDRO-4-(HYDROXYMETHYL)-2H-CYCLOPENTA[B]FURAN-2-ONE;BENZOYL COREY LACTONE;(-)-COREY LACTONE BENZOATE 99%;(-)-COREY LACTONE BENZOATE: (3AR,4S,5R,6AS)-(-)-5-(BENZOYLOXY)-HEXAHYDRO-4(-HYDROXYMETHYL)-2H-CYCLOPENTA[B]FURAN-2-ONE;(-)-6-BETA-HYDROXYMETHYL-7-ALPHA-BENZOYLOXY-CIS-2-OXABICYCLO[3.3.0]OCTAN-3-ONE(COREY''S LACTONE);[3aR-(3aα,4α,5β,6aα)]-5-(Benzoyloxy)hexahydro-4-(hydroxyMethyl)-2H-cyclopenta[b]furan-2-one
CAS:39746-00-4
MF:C15H16O5
MW:276.28
EINECS:254-615-6
Product Categories:Latanoprost;Prostaglandins
Mol File:39746-00-4.mol

(-)-Corey Lactone Benzoate Chemical Properties

Melting point 116-120 °C
alpha -80 º (c=0.8, CHCl3 25 ºC)
Boiling point 379.19°C (rough estimate)
density 1.2379 (rough estimate)
refractive index 1.5000 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka14.79±0.10(Predicted)
color White to Pale Yellow
InChIInChI=1S/C15H16O5/c16-8-11-10-6-14(17)19-12(10)7-13(11)20-15(18)9-4-2-1-3-5-9/h1-5,10-13,16H,6-8H2/t10-,11-,12+,13-/m1/s1
InChIKeyOBRRYUZUDKVCOO-FVCCEPFGSA-N
SMILESO1C(=O)C[C@]2([H])[C@@H](CO)[C@H](OC(=O)C3=CC=CC=C3)C[C@]12[H]
CAS DataBase Reference39746-00-4(CAS DataBase Reference)

Safety Information

Hazard Codes Xn
Risk Statements 22
Safety Statements 36/37/39-26
HS Code 29321900

(-)-Corey Lactone Benzoate Usage And Synthesis

Chemical PropertiesColorless crystalline powder
Uses(-)-Corey Lactone Benzoate is a corey lactone derivative used in the preparation prostaglandin analogues for use as vasolidator as well as EP4 receptor agonists.
Synthesis

39746-01-5

39746-00-4

A 1:1 methanol:methylene chloride solution (40 mL) of (3aR,4R,5R,6aS)-5-(benzoyloxy)hexahydro-2H-cyclopenta[b]furan-2-one-4-carbaldehyde (1) (purchased from Cayman Chemical Company, Ann Arbor, MI) (3.5 g, 12.8 mmol) in a 1:1 methanol:dichloromethane solution (40 mL). After 25 min of reaction, the reaction was quenched by careful addition of saturated aqueous citric acid solution (60 mL). The mixture was extracted with ethyl acetate (3 × 40 mL) and the organic layers were combined and washed sequentially with water (2 × 80 mL) and saturated saline (2 × 80 mL). The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give the target compound 2 (2.43 g, 69% yield).

References[1] Patent: US6353000, 2002, B1. Location in patent: Page column 10
[2] Journal of Pharmacology and Experimental Therapeutics, 1999, vol. 290, # 3, p. 1278 - 1284
[3] Patent: US6353014, 2002, B1. Location in patent: Page column 18

(-)-Corey Lactone Benzoate Preparation Products And Raw materials

Raw materials(-)-3-OXO-6-BETA-TRITYLOXYMETHYL-7-ALPHA-BENZOYL-OXY-2-OXABICYCLO[3.3.0!OCTANE-->(-)-Corey aldehyde benzoate-->Dichloromethane-->Methanol-->Sodium borohydride
Preparation Products(-)-Corey lactone diol-->(-)-3-OXO-6-BETA-TRITYLOXYMETHYL-7-ALPHA-BENZOYL-OXY-2-OXABICYCLO[3.3.0!OCTANE
(-)-Corey lactone 4-phenylbenzoate alcohol CAS 31752-99-5
(-)-Corey lactone diol CAS 32233-40-2
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