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22373-00-8

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22373-00-8 Usage

Description

A homoerythrina type alkaloid also present in Schelhammera pedunculata F. Muell., this base is isomeric with the preceding alkaloid, .differing from it only in the position of the double bond. It is, however, laevorotatory with [α]D - 108° (CHCI3)·

References

Johnsetal., Chem. Commun., 1102 (1968)

Check Digit Verification of cas no

The CAS Registry Mumber 22373-00-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,7 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22373-00:
(7*2)+(6*2)+(5*3)+(4*7)+(3*3)+(2*0)+(1*0)=78
78 % 10 = 8
So 22373-00-8 is a valid CAS Registry Number.

22373-00-8SDS

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 15,16-methanediyldioxy-3α-methoxy-11a-homo-erythrina-1,6-diene

1.2 Other means of identification

Product number -
Other names schelhammeridine

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:22373-00-8 SDS

22373-00-8Downstream Products

22373-00-8Relevant articles and documents

Synthesis of homoerythrinan alkaloids of 1(2)-alkene and 1,6-diene types: Total synthesis of comosine, dihydroschelhammeridine, schelhammeridine, and 3-epischelhammeridine

Tsuda, Yoshisuke,Murata, Masami,Hosoi, Shinzo,Ikeda, Mariko,Sano, Takehiro

, p. 515 - 524 (2007/10/03)

Total syntheses of homoerythrinan alkaloids of 1(2)-alkene type, dihydroschelhammeridine and comosine, and those of 1,6-dienoid type, schelhammeridine and 3-epischelhammeridine, were achieved. Total synthesis of the former alkaloids provided definite proof of their A/B-cis stereochemistry. In relation to the stereochemistry, the conformations of erythrinan and homoerythrinan alkaloids are discussed.

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