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Dispiro[2H-quinolizine-3(4H),2'(3'H)-thiophene- 4'(5'H),3''(4''H)-[2H]quinolizine],6,6''-di-3- furanyldodecahydro-9,9''-dimethyl-,stereoisomer is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67314-63-0

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67314-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67314-63-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,1 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67314-63:
(7*6)+(6*7)+(5*3)+(4*1)+(3*4)+(2*6)+(1*3)=130
130 % 10 = 0
So 67314-63-0 is a valid CAS Registry Number.

67314-63-0SDS

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 (?)-neothiobinupharidine

1.2 Other means of identification

Product number -
Other names neothionuphlutine

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:67314-63-0 SDS

67314-63-0Downstream Products

67314-63-0Relevant academic research and scientific papers

Synthesis of (-)-neothiobinupharidine

Jansen, Daniel J.,Shenvi, Ryan A.

, p. 1209 - 1212 (2013/03/28)

An eight step, asymmetric synthesis of a dimeric thiaspirane nuphar alkaloid from 3-methyl-2-cyclo-pentenone is reported. The brevity of the route relies on a useful procedure for tandem reductive allylation of cyclopentenones, as well as the minimization of redox manipulations and other functional group interconversions. The distribution of products that arise from spontaneous dimerization points to a more complex biosynthesis.

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