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54422-49-0

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54422-49-0 Usage

Description

A glucosidic alkaloid, cadambine occurs in Anthocephalus cadamba. It forms colourless crystals from EtOH and has a specific rotation of [α]D25 - 71 0. It has been characterized as the crystalline tetraacetate with m.p. 149-151 ° C.

References

Brown, Fraser, Tetrahedron Lett., 1957 (1974)

Check Digit Verification of cas no

The CAS Registry Mumber 54422-49-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,2 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54422-49:
(7*5)+(6*4)+(5*4)+(4*2)+(3*2)+(2*4)+(1*9)=110
110 % 10 = 0
So 54422-49-0 is a valid CAS Registry Number.

54422-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Cadambine

1.2 Other means of identification

Product number -
Other names -

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

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More Details:54422-49-0 SDS

54422-49-0Downstream Products

54422-49-0Relevant articles and documents

BIOGENETICALLY PATTERNED SYNTHESIS OF CADAMBINE

Brown, Richard T.,Duckworth, D. Malcolm,Santos, Cid A. M.

, p. 1987 - 1990 (1991)

We report the synthesis of the glucosidic indole alkaloid cadambine (5) in 48 percent yield from its biological precursor secologanin (1) in an intermolecular variant of the in vivo process where chemoselective and regioselective attack by tryptamine on a 3S-epoxide 11 yields the seven-membered azepine ring.

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