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29881-57-0

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29881-57-0 Usage

Description

The leaves and stems of Stemona japonica Miq. contain this alkaloid which is dextrorotatory having [α]D + 273° (MeOH). The ultraviolet spectrum has only a single absorption maximum at 296 mil in EtOIl.

References

Irie et at., Chem. Commun., 1066 (1970)

Check Digit Verification of cas no

The CAS Registry Mumber 29881-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,8 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29881-57:
(7*2)+(6*9)+(5*8)+(4*8)+(3*1)+(2*5)+(1*7)=160
160 % 10 = 0
So 29881-57-0 is a valid CAS Registry Number.

29881-57-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name stemofoline

1.2 Other means of identification

Product number -
Other names 5-((2Z,4S)-8a-butyl-3t-methyl-(3at,8ac)-hexahydro-8t,10at-cyclo-4r,9c-methano-furo[3,2-f]pyrrolo[2,1-c][1,4]oxazepin-2-ylidene)-4-methoxy-3-methyl-5H-furan-2-one

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:29881-57-0 SDS

29881-57-0Downstream Products

29881-57-0Relevant articles and documents

Semi-syntheses of new stemofoline derivatives

Ye, Yang,Velten, Robert F.

, p. 7171 - 7173 (2007/10/03)

Semi-syntheses of several new stemofoline derivatives are described. Acidic hydrolysis of the tetronate moiety of stemofoline, followed by re-esterification gave homologues of stemofoline and isostemofoline. Hydrazinolysis resulted in new pyridazinones. O

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