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85864-86-4

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85864-86-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85864-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,6 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85864-86:
(7*8)+(6*5)+(5*8)+(4*6)+(3*4)+(2*8)+(1*6)=184
184 % 10 = 4
So 85864-86-4 is a valid CAS Registry Number.

85864-86-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-iodonaphthalene-1-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1-formyl-8-iodonaphthalene

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:85864-86-4 SDS

85864-86-4Relevant articles and documents

Synthesis and properties of 9-alkyl- and 9-arylcyclopenta[a]phenalenes

Shea, Kevin M.,Lee, Katherine L.,Danheiser, Rick L.

, p. 2353 - 2356 (2000)

(equation presented) Two strategies for the synthesis of cyclopenta[a]phenalenes are described. NMR, X-ray diffraction, and cyclic voltammetry studies of simple alkyl- and aryl-substituted derivatives are reported for the first time.

Studies in Acyl C-H activation via aryl and alkyl to acyl "through space" migration of palladium

Kesharwani, Tanay,Verma, Akhilesh K.,Emrich, Daniel,Ward, Jeffrey A.,Larock, Richard C.

supporting information; experimental part, p. 2591 - 2593 (2009/10/23)

Examples of the 1,4-migration of a palladium moiety in aryl- and alkylpalladium intermediates to the acyl position of an aldehyde or formamide have been observed. The resulting acylpalladium intermediate can undergo ester or carbamate formation by reaction with an alcohol; decarbonylation, followed by β hydride elimination to an alkene; reaction with an organomercurial to form an ester; or alkene insertion. Deuterium-labeling studies have been used to confirm the palladium migration mechanism.

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