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121219-21-4

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121219-21-4 Usage

Description

1-Octylxy-2,3-difluorobenzene is an organic chemical compound that belongs to the aromatic hydrocarbon family. It is characterized by a benzene ring with two fluorine atoms attached and an octyl group replacing a hydrogen atom. The substitution of hydrogen with the highly electronegative fluorine atoms significantly alters the compound's properties, giving it unique physical and chemical characteristics.

Uses

Used in Chemical Synthesis:
1-Octylxy-2,3-difluorobenzene is used as a chemical intermediate for the synthesis of other chemical substances in scientific research. Its unique properties, resulting from the presence of fluorine atoms and the octyl group, make it a valuable component in the creation of various compounds.
However, it is important to note that the specific applications, toxicity, and environmental impact of 1-Octylxy-2,3-difluorobenzene are not widely studied or documented. Further research is needed to fully understand its potential uses and safety profile in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 121219-21-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,2,1 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 121219-21:
(8*1)+(7*2)+(6*1)+(5*2)+(4*1)+(3*9)+(2*2)+(1*1)=74
74 % 10 = 4
So 121219-21-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H20F2O/c1-2-3-4-5-6-7-11-17-13-10-8-9-12(15)14(13)16/h8-10H,2-7,11H2,1H3

121219-21-4SDS

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 1,2-difluoro-3-octoxybenzene

1.2 Other means of identification

Product number -
Other names 2,3-Difluoro-1-n-octoxybenzene

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:121219-21-4 SDS

121219-21-4Relevant articles and documents

Non-symmetric dimers comprising chalcone and cholesterol entities: An investigation on structure-property correlations

Achalkumar, Ammathnadu S.,Shankar Rao, Doddamane S.,Yelamaggad, Channnabasaveshwar V.

supporting information, p. 4235 - 4248 (2014/11/07)

Four series of new dimers formed by interlinking chalcone and cholesterol mesogenic entities through spacers of varying length and parity have been synthesized and characterized by polarizing optical microscopy, differential scanning calorimetry, X-ray diffraction and electrical switching studies. The structure of the chalcone core has been systematically modified to investigate the effect of the molecular structure on the thermal behaviour of the dimers. The study demonstrates the dramatic dependence of thermal behaviour of these dimers on the nature of the chalcone as well as the length and parity of the spacer. the Partner Organisations 2014.

Influence of fluoro substituents on the mesophase behaviour of banana-shaped molecules

Bedel,Rouillon,Marcerou,Laguerre,Nguyen,Achard

, p. 2214 - 2220 (2007/10/03)

Three new series of bent-shaped five-ring liquid crystals, based on the ester of isophthalic acid as the central core and azomethine linkages, are presented. They differ by the number and the position of halogeno substituents on the outer rings. This lateral substitution strongly influences the type of mesophases formed. Calculations were performed to determine the modification of the distribution of charge along the different molecules.

Mesomorphic di- and tetra-fluorinated imines and their complexes with Re I

Liu, Xiao-Hua,Manners, Ian,Bruce, Duncan W.

, p. 1555 - 1560 (2007/10/03)

The synthesis of some di- and tetra-fluoro imine mesogens is described and their mesomorphism is compared with that of the parent, unfluorinated materials. The comparison reveals that in the fluorinated compounds, more ordered smectic phases were suppress

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