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121051-42-1

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121051-42-1 Usage

Molecular Weight

274.40

Structure

A benzene ring with a dodecyloxy (C12H25O) group attached at the first position and an ethynyl (C2H) group attached at the fourth position.

+ Appearance

Colorless liquid

+ Boiling Point

Approximately 300°C

+ Melting Point

Not available as it is a liquid at room temperature

+ Solubility

Insoluble in water, soluble in organic solvents such as ethanol, dichloromethane, and acetone.

+ Reactivity

Can undergo addition reactions with various reagents, such as hydrogen, halogens, and metal hydrides.

+ Stability

Stable under normal conditions, but can be oxidized or reduced under certain conditions.

+ Organic Synthesis

Used as a building block for the creation of more complex molecules.

+ Materials Science

Used in the production of liquid crystals and as a functional material in various electronic devices.

Importance

Its unique structure and properties make it a valuable compound for research and development in the field of organic chemistry and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 121051-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,0,5 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 121051-42:
(8*1)+(7*2)+(6*1)+(5*0)+(4*5)+(3*1)+(2*4)+(1*2)=61
61 % 10 = 1
So 121051-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H30O/c1-3-5-6-7-8-9-10-11-12-13-18-21-20-16-14-19(4-2)15-17-20/h2,14-17H,3,5-13,18H2,1H3

121051-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-dodecoxy-4-ethynylbenzene

1.2 Other means of identification

Product number -
Other names 1-dodecyloxy-4-methoxybenzene

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:121051-42-1 SDS

121051-42-1Relevant articles and documents

Pi-Extended Ethynyl 21,23-Dithiaporphyrins: A Synthesis and Comparative Study of Electrochemical, Optical, and Self-Assembling Properties

Bromby, Ashley D.,Keller, Samantha N.,Bozek, Kevin J. A.,Williams, Vance E.,Sutherland, Todd C.

, p. 9401 - 9409 (2015)

21,23-Dithiaporphyrins were synthesized containing pi-extending ethynyl substituents at the meso positions. These porphyrins displayed highly bathochromic and broadened absorbance profiles spanning 400-900 nm with molar absorptivities ranging from 2500 to 300,000 M-1 cm-1. Electrochemically, these ethynyl dithiaporphyrins undergo a single oxidation at 0.44 or 0.57 V and reduction at -1.17 or -1.08 V versus a ferrocene/ferrocenium internal standard depending on the type of functionalization appended to the ethynyl group. DFT calculations predict that the delocalization of the frontier molecular orbitals should expand onto the meso positions of the ethynyl 21,23-dithiaporphyrins; shrinking the HOMO-LUMO energy gap by destabilizing the HOMO energy. Indeed, the DFT results agree with our optical and electrochemical assessments. Finally, differential scanning calorimetry combined with cross-polarized optical microscopy and powder X-ray diffraction was used to assess the ability of these porphyrins for long-range order. For the ethynylphenyl alkoxy 21,23-dithiaporphyin, birefringent, soft-crystalline-like domains were observed by polarized microscopy, which are marginally sustained by a low-level of crystallinity detected in the XRD, suggesting that long-range ordering is possible. Overall, ethynyl 21,23-dithiaporphyrins are able to harvest much lower energy light and possess lower oxidation and reduction potentials compared to their pyrrolic analogues, which are desirable properties for applications in organic electronics.

Synthesis, mesomorphism, photophysics and device performance of liquid-crystalline pincer complexes of gold(iii)

Parker, Rachel R.,Liu, Denghui,Yu, Xiankang,Whitwood, Adrian C.,Zhu, Weiguo,Williams,Wang, Yafei,Lynam, Jason M.,Bruce, Duncan W.

, p. 1287 - 1302 (2021/02/12)

Emissive gold(iii) complexes of pincer 2,6-diphenylpyridines also bearing a phenylacetylide ligand have been modified at both the pincer and phenylacetylide to confer liquid crystalline properties, with most complexes showing a columnar hexagonal phase in

Thermal and nonlinear optical studies of newly synthesized EDOT based bent-core and hockey-stick like liquid crystals

Gowda, Ashwathanarayana,Jacob, Litwin,Joy, Nithin,Philip, Reji,Pratibha,Kumar, Sandeep

, p. 2047 - 2057 (2018/02/09)

Novel EDOT based bent-core and hockey-stick shaped mesogens bearing terminal alkyl chains and alkoxy terminal chains, respectively, have been designed and synthesized via the Sonogashira coupling reaction. Molecular structures of these new compounds were

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