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1,3-Cyclopentadiene, 1,4-bis(1,1-dimethylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34671-24-4

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34671-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34671-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,7 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34671-24:
(7*3)+(6*4)+(5*6)+(4*7)+(3*1)+(2*2)+(1*4)=114
114 % 10 = 4
So 34671-24-4 is a valid CAS Registry Number.

34671-24-4SDS

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 1,3-di-(tert-butyl)-cyclopentadiene

1.2 Other means of identification

Product number -
Other names 1,3-di(tert-butyl)cyclopentadiene

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:34671-24-4 SDS

34671-24-4Downstream Products

34671-24-4Relevant academic research and scientific papers

Synthesis and properties of sterically congested cyclopentadienes and their transition metal complexes

Clark, T. Jeffrey,Killian, Christopher M.,Luthra, Sanjay,Nile, Terence A.

, p. 247 - 258 (2007/10/02)

The synthesis of 1,3-dialkyl substituted cyclopentadienes, C5H4RR', Cp'H (Va-g) (where R and R' are tert-butyl, iso-propyl, neo-pentyl, cyclohexyl, or 1-methylcyclohexyl) is reported.These are synthesized by the nucleophilic addition of methyl or hydride anions to the corresponding 2-alkyl-6,6-dialkylfulvenes (IIIa-f) followed by hydrolysis.These substituted 1,3-cyclopentadienes have been converted to organometallic derivatives such as 2, (M=Mo or W) and Cp'2Fe.The spectroscopic and electrochemical properties of selected complexes have been investigated to probe the steric and electronic properties of the substituted cyclopentadienyl ligands.

PHASE TRANSFER CATALYZED TERT-ALKYLATIONS OF CYCLOPENTADIENE AND INDENE: INDICATIONS FOR SET PROCESSES

Dehmlow, Eckehard V.,Bollmann, Christof

, p. 5773 - 5776 (2007/10/02)

Scope and mechanism of the PTC tert-alkylation of cyclopentadienide anion have been investigated.On the side of the anion, the reaction is limited to cyclopentadiene and indene, whereas many tertiary as well as secondary and primary alkylating agents can be employed.Hexamethylcyclopentadiene 8, for instance, is available easily.Tert-alkylations of this type are more effective if 4,4'-bipyridinium salts are present in addition to a phase transfer catalyst.The reactions involve probably an initial single electron transfer (SET) step.

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