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Cyclopentanone, 2,2'-[1,5-bis(2-methoxyphenyl)-3-oxo-1,5-pentanediyl]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67860-98-4

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67860-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67860-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,6 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67860-98:
(7*6)+(6*7)+(5*8)+(4*6)+(3*0)+(2*9)+(1*8)=174
174 % 10 = 4
So 67860-98-4 is a valid CAS Registry Number.

67860-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-(1,5-bis(2-methoxyphenyl)-3-oxopentane-1,5-diyl)dicyclopentanone

1.2 Other means of identification

Product number -
Other names -

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:67860-98-4 SDS

67860-98-4Downstream Products

67860-98-4Relevant academic research and scientific papers

Reaction of Enamines with Dibenzylideneacetone - Solvent Effect and Electron Impact Study

Rao, T. Vedagiriswara,Anandan, Lalitha,Mathur, H. H.,Trivedi, G. K.

, p. 864 - 867 (2007/10/02)

The Stork addition of the pyrrolidineenamines of cycloalkanones (Ia-d) to dibenzylideneacetones (IIa-c) in ethanol media at room temperature, followed by heating briefly at reflux, results either in bis-adducts (IIIa-c) and/or bridged bicyclic diketones (IVa-c), which contain the rare bicyclodecane ring system.The proposed structures of the products have been fully corroborated by their mass fragmentation pattern.

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