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2-Propanone, 1,3-bis(1-methyl-2-pyrrolidinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

46727-05-3

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46727-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 46727-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,7,2 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 46727-05:
(7*4)+(6*6)+(5*7)+(4*2)+(3*7)+(2*0)+(1*5)=133
133 % 10 = 3
So 46727-05-3 is a valid CAS Registry Number.

46727-05-3SDS

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 1,3-bis-(1-methyl-pyrrolidin-2-yl)-propan-2-one

1.2 Other means of identification

Product number -
Other names cuscohygrine

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:46727-05-3 SDS

46727-05-3Downstream Products

46727-05-3Relevant academic research and scientific papers

Chemotaxonomy of the pantropical genus Merremia (Convolvulaceae) based on the distribution of tropane alkaloids

Jenett-Siems, Kristina,Weigl, Robert,Boehm, Anke,Mann, Petra,Tofern-Reblin, Britta,Ott, Sonja C.,Ghomian, Azar,Kaloga, Maki,Siems, Karsten,Witte, Ludger,Hilker, Monika,Mueller, Frank,Eich, Eckart

, p. 1448 - 1464 (2005)

The occurrence and distribution of tropane and biogenetically related pyrrolidine alkaloids in 18 Merremia species of paleo-, neo-, and pantropical occurrence have been studied. The extensive GC-MS study included members of almost all sections of the genu

Total synthesis of (+)-dihydrocuscohygrine and cuscohygrine

Stapper, Christian,Blechert, Siegfried

, p. 6456 - 6460 (2007/10/03)

The first enantioselective synthesis of (+)-dihydrocuscohygrine 1 and cuscohygrine 2 is presented. 1 was obtained in nine steps and 30% overall yield with a ruthenium-catalyzed tandem ring rearrangement metathesis key step starting from enantiomerically pure cycloheptene-1,3,5-triol derivative 6. The unknown absolute configuration of natural dihydrocuscohygrine 1 could be determined as (S,S)-(-). Cuscohygrine 2 was obtained by Jones oxidation of 1 in quantitative yield but unfortunately with complete epimerization.

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