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30333-81-4

30333-81-4

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30333-81-4 Usage

Description

This alkaloid has been isolated by Russian workers from Dipsacus azureus Schrenk, who give it the empirical formula CllH13N0 3 and the structure shown above.

References

Rakhmatullaev, Yunusov, Khim. Prir. Soedin., 8, 400 (1972)

Check Digit Verification of cas no

The CAS Registry Mumber 30333-81-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,3 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30333-81:
(7*3)+(6*0)+(5*3)+(4*3)+(3*3)+(2*8)+(1*1)=74
74 % 10 = 4
So 30333-81-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO3/c1-6-8-4-12-5-9(11(14)15-2)7(8)3-10(6)13/h4-6,10,13H,3H2,1-2H3/t6-,10+/m1/s1

30333-81-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (6S,7R)-6-hydroxy-7-methyl-6,7-dihydro-5H-cyclopenta[c]pyridine-4-carboxylate

1.2 Other means of identification

Product number -
Other names Cantleyine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:30333-81-4 SDS

30333-81-4Downstream Products

30333-81-4Relevant articles and documents

174. Plantes de Nouvelle-Caledonie 94e Communication Alcaloides monoterpeniques de Scaevola racemigera Daeniker

Skaltsounis, Alexios-Leandros,Michel, Sylvie,Tillequin, Francois,Koch, Michel,Pusset, Jacques,Chauviere, Gerard

, p. 1679 - 1685 (2007/10/02)

Nine alkaloids have been isolated from the aerial parts of Scaevola racemigera.Two of them are known compounds cantleyine (1) and tetrahydrocantleyine (2).The seven others are novel alkaloids, strychnovoline (3), 6-O-nicotinoylstrychnovoline (4), 6-O-nicotinoyltetrahydrocantleyine (5), 6-O-(5-vinylnicotinoyl)tetrahydrocantleyine (6), racemigerine (7), 6,7-epoxyracemigerine (8), and scaevoline (9).The structures of the new compounds have been elucidated by their spectral data and confirmed by chemical correlations.Moreover, the absolute configuration of 2, which had not been previously determined, has been elucidated.

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