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77785-81-0

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77785-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77785-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,7,8 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77785-81:
(7*7)+(6*7)+(5*7)+(4*8)+(3*5)+(2*8)+(1*1)=190
190 % 10 = 0
So 77785-81-0 is a valid CAS Registry Number.

77785-81-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[7-(3,4-dicyanophenoxy)naphthalen-2-yl]oxybenzene-1,2-dicarbonitrile

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:77785-81-0 SDS

77785-81-0Downstream Products

77785-81-0Relevant articles and documents

Nitrodisplacement reactions and the synthesis of bis (ether anhydride) s from dihydroxynaphthalenes

Eastmond, Geoffrey C.,Paprotny, Jerzy

, p. 1455 - 1458 (2007/10/03)

Nitrodisplacement reactions between all ten dihydroxynaphthalenes and 4-nitrophthalodinitrile have been studied. Apart from 1,8-dihydroxynaphthalene, all dihydroxynaphthalenes undergo nitrodisplacement but only 1,5-, 2,3-, 2,6- and 2,7-dihydroxynaphthalenes give high yields of pure bis(ether dinitrile). The bis(ether dinitrile)s produced in high yield were hydrolysed and converted to bis(ether anhydride) for subsequent synthesis of poly (ether imide)s. Success in nitrodisplacement correlates with high redox potentials for the dihydroxynaphthalenes, except for 1,8-dihydroxynaphthalene which probably fails to react because of steric constraints at the peri positions.

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