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2-Heptene, 2,4-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

860116-58-1

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860116-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 860116-58-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,0,1,1 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 860116-58:
(8*8)+(7*6)+(6*0)+(5*1)+(4*1)+(3*6)+(2*5)+(1*8)=151
151 % 10 = 1
So 860116-58-1 is a valid CAS Registry Number.

860116-58-1SDS

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 2,4-dimethylhept-2-ene

1.2 Other means of identification

Product number -
Other names 2,3-Dimethyl-2-hepten

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:860116-58-1 SDS

860116-58-1Upstream product

860116-58-1Downstream Products

860116-58-1Relevant academic research and scientific papers

Reactions of Propene on Zeolite HY Catalyst Studied by in Situ Variable-Temperature Solid-State Nuclear Magnetic Resonance Spectroscopy

Haw, James F.,Richardson, Benny R.,Oshiro, Irene S.,Lazo, Noel D.,Speed, James A.

, p. 2052 - 2058 (1989)

The oligomerization reactions of propene on zeolite catalyst HY have been studied in detail by in situ variable-temperature 13C solid-state NMR with cross polarization (CP) and magic-angle spinning (MAS).Propene is shown to be highly mobile in the zeolite at temperature far below the onset of chemical reactivity.Alkoxy species formed between protonated alkenes and zeolite framework oxygens are found to be important long-lived intermediates in the reactions.Simple secondary or tertiary carbocations either do not exist as free ions in the zeolite at low temperature or are so transient that they are not detected by NMR even at temperatures as low as 163 K.There is, however, evidence for long-lived alkyl-substituted cyclopentenyl carbocations, which are formed as free ions in the zeolite at room temperature.These carbocations do not form until all of the propene is consumed and hence do not play a significant role in the oligomerization reactions.A detailed reaction mechanism is proposed to account for all of the experimental observations.Novel experimental techniques are introduced which will be applicable to the study of many highly reactive catalyst/adsorbate systems.

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