Paniculidine B | CAS:97399-94-5 | Manufacturer ChemFaces

Paniculidine B

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Paniculidine B 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]

METHODS AND RESULTS:
A general route to 2-unsubstituted-1-methoxyindoles, based on our methodology for the synthesis of 1-methoxyindoles, is reported. 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.

Chemical & Pharmaceutical Bulletin , 1985 , 33 (4) :1770-3

Structures of paniculidines A and B: novel prenylindoles from Murraya paniculata[Reference: WebLink]

METHODS AND RESULTS:
Two new indoles named Paniculidine A and Paniculidine B were isolated from Murraya paniculata (Linn.) Jack., and their structures have been elucidated as methyl 2-methyl-4-(indol-3-yl)-butyrate and 2-methyl-4-(1-methoxyindol-3-yl)-1-butanol, respectively.

Product Name	Paniculidine B
Price:
CAS No.:	97399-94-5
Catalog No.:	CFN97553
Molecular Formula:	C₁₄H₁₉NO₂
Molecular Weight:	233.3 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	4.2863 mL	21.4316 mL	42.8633 mL	85.7265 mL	107.1582 mL
5 mM	0.8573 mL	4.2863 mL	8.5727 mL	17.1453 mL	21.4316 mL
10 mM	0.4286 mL	2.1432 mL	4.2863 mL	8.5727 mL	10.7158 mL
50 mM	0.0857 mL	0.4286 mL	0.8573 mL	1.7145 mL	2.1432 mL
100 mM	0.0429 mL	0.2143 mL	0.4286 mL	0.8573 mL	1.0716 mL

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
CFN97552	Paniculidine A	97399-93-4	231.3	C₁₄H₁₇NO₂
CFN97553	Paniculidine B	97399-94-5	233.3	C₁₄H₁₉NO₂
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