Paniculidine C | CAS:97399-95-6 | Manufacturer ChemFaces

Paniculidine C

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Paniculidine C Description

Source:	The herbs of Murraya exotica 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:

J Org Chem. 2004 Jun 25;69(13):4429-32.

Efficient total syntheses of phytoalexin and (+/-)-paniculidine B and C based on the novel methodology for the preparation of 1-methoxyindoles.[Pubmed: 15202897 ]

A general route to 2-unsubstituted-1-methoxyindoles, based on our methodology for the synthesis of 1-methoxyindoles, is reported.
METHODS AND RESULTS:
This synthesis renders accessibility to a variety of natural products possessing the said skeleton. A direct synthesis of phytoalexin (1), (+/-)-paniculidine B (2), and (+/-)-Paniculidine C (3) is disclosed based on the methodology.
CONCLUSIONS:
The synthesis of paniculidine B (2) has been achieved from aldehyde 10 in only two steps in 88% yield and in five steps from a methoxyindole compound 8 obtained using our earlier methodology.

Product Name	Paniculidine C
Price:
CAS No.:	97399-95-6
Catalog No.:	CFN97554
Molecular Formula:	C₁₃H₁₇NO
Molecular Weight:	203.3 g/mol
Purity:	>=98%
Type of Compound:	Alkaloids
Physical Desc.:	Oil
Source:	The herbs of Murraya exotica 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	Alkaloids Compound Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	4.9188 mL	24.5942 mL	49.1884 mL	98.3768 mL	122.971 mL
5 mM	0.9838 mL	4.9188 mL	9.8377 mL	19.6754 mL	24.5942 mL
10 mM	0.4919 mL	2.4594 mL	4.9188 mL	9.8377 mL	12.2971 mL
50 mM	0.0984 mL	0.4919 mL	0.9838 mL	1.9675 mL	2.4594 mL
100 mM	0.0492 mL	0.2459 mL	0.4919 mL	0.9838 mL	1.2297 mL

CFN97554	Paniculidine C	97399-95-6	203.3	C₁₃H₁₇NO
CFN99899	Indole-3-acrylic acid methyl ester	19626-92-7	201.2	C₁₂H₁₁NO₂
CFN95263	Indolelactic acid	1821-52-9	205.2	C₁₁H₁₁NO₃
CFN97559	Methyl 3-carbazolecarboxylate	97931-41-4	225.2	C₁₄H₁₁NO₂
CFN91466	Mukonine	23523-94-6	255.3	C₁₅H₁₃NO₃
CFN97256	1H-Indole-3-carboxylic acid	771-50-6	161.2	C₉H₇NO₂
CFN97515	Methyl 3-indolecarboxylate	942-24-5	175.2	C₁₀H₉NO₂
CFN96192	2-(1H-Indole-3-carboxamido)benzoic acid	171817-95-1	280.3	C₁₆H₁₂N₂O₃
CFN91534	Cephalandole B	915315-44-5	294.3	C₁₇H₁₄N₂O₃
CFN96487	Indole-3-glyoxylamide	5548-10-7	188.18	C₁₀H₈N₂O₂