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5-Dehydrosparteine is a naturally occurring quinolizidine alkaloid found in the plant genus Lupinus. It is structurally similar to sparteine, differing only by the presence of a double bond between carbons 5 and 6. 5-dehydrosparteine exhibits various pharmacological properties, such as antiarrhythmic, antispasmodic, and anti-inflammatory effects. 5-Dehydrosparteine has been studied for its potential applications in treating cardiovascular diseases and neurological disorders. However, due to its complex structure and limited availability, further research is needed to fully understand its therapeutic potential and safety profile.

2130-67-8

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2130-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2130-67-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,3 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2130-67:
(6*2)+(5*1)+(4*3)+(3*0)+(2*6)+(1*7)=48
48 % 10 = 8
So 2130-67-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H24N2/c1-3-7-16-11-13-9-12(14(16)5-1)10-17-8-4-2-6-15(13)17/h5,12-13,15H,1-4,6-11H2/t12-,13-,15-/m0/s1

2130-67-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-Didehydrosparteine

1.2 Other means of identification

Product number -
Other names 5-Dehydrosparteine

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:2130-67-8 SDS

2130-67-8Downstream Products

2130-67-8Relevant academic research and scientific papers

Kinetic Resolution of Racemic α-Methylbenzyl Methacrylate: Asymmetric Selective Polymerization Catalyzed by Grignard Reagent-(-)-Sparteine Derivative

Okamoto, Yoshio,Suzuki, Koichi,Kitayama, Tatsuki,Yuki, Heimei,Kageyama, Hiroyuki,at al.

, p. 4618 - 4624 (2007/10/02)

Enantiomer-selective polymerization of racemic (RS)-α-methylbenzyl methacrylate (MBMA) was investigated with homogeneous Grignard reagent-(-)-sparteine and its derivative catalysts in toluene at -78 deg C.A variety of Grignard reagents (RMgX) were combine

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