3-Hydroxymollugin | CAS:154706-45-3 | Manufacturer ChemFaces

3-Hydroxymollugin

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3-Hydroxymollugin Description

Source:	The roots of Pentas longiflora.
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

Structure Identification:

J Org Chem . 2010 Apr 2;75(7):2274-2280.

Synthesis of the natural products 3-hydroxymollugin and 3-methoxymollugin[Pubmed: 20201485]

3-Hydroxymollugin 2 and 3-methoxymollugin 3 are cytotoxic compounds isolated as minor compounds from Pentas longiflora and Rubia cordifolia. Syntheses of 3-Hydroxymollugin 2 and 3-methoxymollugin 3 were developed starting from easily available 3-bromomollugin 6. Surprisingly, it was found that the reaction of 3-bromomollugin 6 with sodium methoxide in methanol resulted in the formation of 3-methoxymollugin 3 and the ring-contracted methyl isopropenylfuromollugin 7. A mechanism for this ring contraction is proposed on the basis of a pericyclic retro oxa-6pi ring-opening reaction. A second synthesis of 3-Hydroxymollugin 2 was based on epoxidation of methyl 3-(3-methylbut-2-enyl)-1,4-naphthoquinone-2-carboxylate 17 and subsequent reduction of the quinone moiety, ring transformation, and DDQ oxidation. The latter oxidation process results in 3-Hydroxymollugin 2 along with the rearranged furomollugin 4, which is a ring-contracted analogue of the natural product mollugin 1.

Product Name	3-Hydroxymollugin
Price:	$368 / 5mg
CAS No.:	154706-45-3
Catalog No.:	CFN95424
Molecular Formula:	C₁₇H₁₆O₅
Molecular Weight:	300.3 g/mol
Purity:	>95%
Type of Compound:	Phenols
Physical Desc.:	Powder
Source:	The roots of Pentas longiflora.
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download:	COA MSDS
Similar structural:	Comparison (Web) (SDF)
Guestbook:

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Phenols Compound Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	3.33 mL	16.65 mL	33.3 mL	66.6001 mL	83.2501 mL
5 mM	0.666 mL	3.33 mL	6.66 mL	13.32 mL	16.65 mL
10 mM	0.333 mL	1.665 mL	3.33 mL	6.66 mL	8.325 mL
50 mM	0.0666 mL	0.333 mL	0.666 mL	1.332 mL	1.665 mL
100 mM	0.0333 mL	0.1665 mL	0.333 mL	0.666 mL	0.8325 mL

CFN98441	Catalponol	34168-56-4	230.3	C₁₅H₁₈O₂
CFN98311	3-Hydroxycatalponol	265644-24-4	246.3	C₁₅H₁₈O₃
CFN99688	1-Hydroxy-2-prenylnaphthalene	16274-34-3	212.3	C₁₅H₁₆O
CFN99687	3,4-Dihydro-2,2-dimethyl-2H-naphtho[1,2-b]pyran	16274-33-2	212.3	C₁₅H₁₆O
CFN98930	Mollugin	55481-88-4	284.3	C₁₇H₁₆O₄
CFN95424	3-Hydroxymollugin	154706-45-3	300.3	C₁₇H₁₆O₅
CFN96857	3-Methoxymollugin	154706-44-2	314.33	C₁₈H₁₈O₅
CFN91030	Dihydromollugin	60657-93-4	286.32	C₁₇H₁₈O₄
CFN96847	Nonin A	1357351-29-1	300.31	C₁₇H₁₆O₅
CFN97055	Furomollugin	61658-41-1	242.2	C₁₄H₁₀O₄