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Benzene, hexakis(1-methylethyl)-, also known as hexamethylbenzene or 1,2,3,4,5,6-hexamethylbenzene, is an organic compound with the chemical formula C12H18. It is a symmetrical, highly branched alkane with a benzene ring structure, where each carbon atom on the ring is substituted with a methyl group (CH3). Benzene, hexakis(1-methylethyl)- is a colorless, crystalline solid with a melting point of 165-166°C and a boiling point of 269-270°C. Hexamethylbenzene is insoluble in water but soluble in most organic solvents. It is used as a chemical intermediate in the synthesis of various compounds, such as dyes, pharmaceuticals, and polymers, and also serves as a solvent and a ligand in coordination chemistry. Due to its low toxicity and stable nature, hexamethylbenzene is considered a relatively safe chemical, but it should still be handled with care to avoid potential health and environmental risks.

800-12-4

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800-12-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 800-12-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,0 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 800-12:
(5*8)+(4*0)+(3*0)+(2*1)+(1*2)=44
44 % 10 = 4
So 800-12-4 is a valid CAS Registry Number.

800-12-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,5,6-hexa(propan-2-yl)benzene

1.2 Other means of identification

Product number -
Other names hexaisopropylbenzene

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:800-12-4 SDS

800-12-4Upstream product

800-12-4Downstream Products

800-12-4Relevant academic research and scientific papers

The first cobalt catalyzed [2 + 2 + 2] alkyne cyclotrimerization in aqueous medium at room temperature

Yong, Li,Butenschoen, Holger

, p. 2852 - 2853 (2002)

Chelate complex 1 (5 mol%) was found to catalyze the [2 + 2 + 2] cyclization of terminal alkynes in good yields in a 80/20 mixture of water and ethanol at room temperature without further activation.

Static and Dynamic Stereochemistry of Hexaisopropylbenzene: A Gear-Meshed Hydrocarbon of Exceptional Rigidity

Siegel, Jay,Gutierrez, Alberto,Schweizer, W. Bernd,Ermer, Otto,Mislow, Kurt

, p. 1569 - 1575 (1986)

The crystal and molecular structure of hexaisopropylbenzene (1) has been analyzed by X-ray methods at 99 K: space group P1/, a = 6.400(2) Angstroem, b = 9.943(3) Angstroem, c = 10.223(2) Angstroem α = 117.79(2) deg, β = 94.78(3) deg, γ = 105.58(3) deg, Z = 1.The molecules closely approximate C6h symmetry in the crystal.A crystallographic orientational disorder around the molecular sixfold axes was modeled with the help of simple structural and geometrical considerations.The molecular model thus derived accords well with the C6h ground state calculated by the empirical force field (EFF) method.The relative energies of the nine conformers of 1 have been estimated by EFF calculations, and a one-to-one mapping of the conformers of 1 and hexaethylbenzene is developed.An improved approach for the synthesis of 1 has been devised, based on a novel method for obtaining the precursor, diisopropylacetylene.Cotrimerization of diisopropylacetylene with an elevenfold molar excess of diisopropylacetylene-d14 in the presence of Hg2 gives a mixture of isotopomers in which 1-d28 is the major isomer observable by 1H NMR spectroscopy.From the noncoalescence of the resonance-doubled signals of methyl and methine protons, a ΔG* value of ae 22 kcal mol-1 is estimated for the process of internal rotation in 1.EFF calculations serve to rule out correlated rotation of the isopropyl groups.A reaction graph for stepwise rotation has been constructed and saddle points calculated for the individual transitions.These calculations indicate that the process of homomerization by rotation of all six isopropyl groups requires ca. 35 kcal mol-1.

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