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466-69-3

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466-69-3 Usage

Chemical class

Alkaloid

Source

Plant Strychnos nux-vomica

Common use

Pesticide and rodenticide

Structure

Complex and intricate, containing multiple ring systems and functional groups

Toxicity

Potent neurotoxin

Regulation

Highly regulated, use restricted to licensed professionals

Handling

Must be handled with extreme caution due to potential harm to human and animal health.

Check Digit Verification of cas no

The CAS Registry Mumber 466-69-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 466-69:
(5*4)+(4*6)+(3*6)+(2*6)+(1*9)=83
83 % 10 = 3
So 466-69-3 is a valid CAS Registry Number.

466-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tetranitrobenzo-18-crown-6

1.2 Other means of identification

Product number -
Other names 4,4',5,5'-Tetranitrodibenzo-18-crown-6

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:466-69-3 SDS

466-69-3Downstream Products

466-69-3Relevant articles and documents

Structure-activity relationships of strychnine analogs at glycine receptors

Mohsen, Amal M. Y.,Heller, Eberhard,Holzgrabe, Ulrike,Jensen, Anders A.,Zlotos, Darius P.

, p. 1256 - 1262 (2014/10/16)

Nine strychnine derivatives including neostrychnine, strychnidine, isostrychnine, 21,22-dihydro-21-hydroxy-22-oxo-strychnine, and several hydrogenated analogs were synthesized, and their antagonistic activities at human α1 and α1β glycine receptors were evaluated. Isostrychnine has shown the best pharmacological profile exhibiting an IC 50 value of 1.6μM at α1 glycine receptors and 3.7-fold preference towards the α1 subtype. SAR Analysis indicates that the lactam moiety and the C(21) C(22) bond in strychnine are essential structural features for its high antagonistic potency at glycine receptors Copyright

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