Rutaretin | CAS:13895-92-6 | Manufacturer ChemFaces

Rutaretin

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Rutaretin Description

Source:	The herbs of Ruta graveolens L.
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:

Tetrahedron.1981;37(2):285-290.

Studies on the chemical constituents of rutaceous plants—XLI : Absolute configuration of rutaretin methyl ether.[Reference: WebLink]

METHODS AND RESULTS:
The absolute configuration of Rutaretin methylether(1) has been established by transformation of it into methyl hexahydroRutaretin methyl ether (5) which was independently derived from S-marmesin (2) via photo-Fries reaction as a key step.

Nat Prod Res. 2004 Apr;18(2):141-6.

Marmenol: a 7-geranyloxycoumarin from the leaves of Aegle marmelos Corr.[Pubmed: 14984087 ]

METHODS AND RESULTS:
A new 7-geranyloxycoumarin [7-(2,6-dihydroxy-7-methoxy-7-methyl-3-octaenyloxy) coumarin] named marmenol (1) has been isolated from the leaves of methanolic extract of Aegle marmelos belonging to the family Rutaceae. In addition to marmenol, several known compounds have also been obtained for the first time from the same source. They include: praealtin D, trans-cinnamic acid, valencic acid, 4-methoxy benzoic acid, betulinic acid, N-p-cis- and trans-coumaroyltyramine, montanine, and Rutaretin.
CONCLUSIONS:
The structures of marmenol and known constituents were established with the help of NMR spectroscopy. However, structure of 1 was further confirmed via 2-D NMR experiments.

Product Name	Rutaretin
Price:
CAS No.:	13895-92-6
Catalog No.:	CFN97825
Molecular Formula:	C₁₄H₁₄O₅
Molecular Weight:	262.26 g/mol
Purity:	>=98%
Type of Compound:	Coumarins
Physical Desc.:	Powder
Source:	The herbs of Ruta graveolens L.
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download:	COA MSDS SDF
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	Coumarins Compound Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	3.813 mL	19.065 mL	38.1301 mL	76.2602 mL	95.3252 mL
5 mM	0.7626 mL	3.813 mL	7.626 mL	15.252 mL	19.065 mL
10 mM	0.3813 mL	1.9065 mL	3.813 mL	7.626 mL	9.5325 mL
50 mM	0.0763 mL	0.3813 mL	0.7626 mL	1.5252 mL	1.9065 mL
100 mM	0.0381 mL	0.1907 mL	0.3813 mL	0.7626 mL	0.9533 mL

CFN80120	Marmesin angelate	13209-79-5	328.36	C₁₉H₂₀O₅
CFN92711	Ammijin	495-30-7	408.4	C₂₀H₂₄O₉
CFN90232	Nodakenin	495-31-8	408.40	C₂₀H₂₄O₉
CFN95202	6'-Feruloylnodakenin	131623-14-8	584.6	C₃₀H₃₂O₁₂
CFN95004	Decuroside I	96638-79-8	570.6	C₂₆H₃₄O₁₄
CFN97442	Smyrindioloside	87592-77-6	424.4	C₂₀H₂₄O₁₀
CFN98907	2-(1-Hydroxy-1-methylethyl)-4-methoxy-7H-furo[3,2-g][1]benzopyran-7-one	54087-32-0	274.3	C₁₅H₁₄O₅
CFN97825	Rutaretin	13895-92-6	262.26	C₁₄H₁₄O₅
CFN92800	Qianhucoumarin G	68692-61-5	262.3	C₁₄H₁₄O₅
CFN98788	Nodakenetin	495-32-9	246.3	C₁₄H₁₄O₄