Welcome to LookChem.com Sign In|Join Free

CAS

  • or
1-Heptyloxy-2,3-difluorobenzene, with the molecular formula C11H15F2O, is a colorless liquid chemical compound characterized by a molecular weight of 198.23 g/mol. It serves as a versatile building block in the synthesis of a variety of organic compounds and materials, owing to its unique structure and properties.

122265-84-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 122265-84-3 Structure
  • Basic information

    1. Product Name: 1-Heptyloxy-2,3-difluorobenzene
    2. Synonyms: 1-Heptyloxy-2,3-difluorobenzene;1,2-Difluoro-3-(heptyloxy)benzene;Benzene, 1,2-difluoro-3-(heptyloxy)-
    3. CAS NO:122265-84-3
    4. Molecular Formula: C13H18F2O
    5. Molecular Weight: 228.28
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 122265-84-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 268.416 °C at 760 mmHg
    3. Flash Point: 123.429 °C
    4. Appearance: /
    5. Density: 1.033 g/cm3
    6. Vapor Pressure: 0.0127mmHg at 25°C
    7. Refractive Index: 1.461
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-Heptyloxy-2,3-difluorobenzene(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-Heptyloxy-2,3-difluorobenzene(122265-84-3)
    12. EPA Substance Registry System: 1-Heptyloxy-2,3-difluorobenzene(122265-84-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 122265-84-3(Hazardous Substances Data)

122265-84-3 Usage

Uses

Used in Pharmaceutical Industry:
1-Heptyloxy-2,3-difluorobenzene is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 1-Heptyloxy-2,3-difluorobenzene is utilized as a precursor in the production of agrochemicals, aiding in the creation of compounds that can enhance crop protection and yield.
Used in Specialty Chemicals Industry:
1-Heptyloxy-2,3-difluorobenzene is employed as a valuable intermediate in the synthesis of specialty chemicals, where its distinctive structure allows for the production of high-performance materials for various applications.
It is crucial to handle 1-Heptyloxy-2,3-difluorobenzene with caution due to its potential health hazards if not used or stored properly, emphasizing the need for safe practices in its application across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 122265-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,2,6 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 122265-84:
(8*1)+(7*2)+(6*2)+(5*2)+(4*6)+(3*5)+(2*8)+(1*4)=103
103 % 10 = 3
So 122265-84-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H18F2O/c1-2-3-4-5-6-10-16-12-9-7-8-11(14)13(12)15/h7-9H,2-6,10H2,1H3

122265-84-3SDS

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 1,2-difluoro-3-heptoxybenzene

1.2 Other means of identification

Product number -
Other names 1,2-difluoro-3-n-heptyloxybenzene

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:122265-84-3 SDS

122265-84-3Synthetic route

1-Bromoheptane
629-04-9

1-Bromoheptane

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

Conditions
ConditionsYield
With potassium carbonate In butanone Heating / reflux;97%
With potassium carbonate In ethyl acetate Heating;90%
With potassium carbonate In acetone for 48h; Alkylation; Heating;
With potassium hydroxide In ethanol
With sodium hydroxide In dimethyl sulfoxide
ortho-difluorobenzene
367-11-3

ortho-difluorobenzene

2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1.1: n-butyllithium / hexane; tetrahydrofuran / 2.5 h / -78 °C
1.2: hexane; tetrahydrofuran / -78 - 20 °C
2.1: 100 percent / 10 percent aq. HCl / 1 h / 20 °C
3.1: 100 percent / 10 percent aq. H2O2 / diethyl ether / 2.5 h / Heating
4.1: K2CO3 / acetone / 48 h / Heating
View Scheme
(2,3-difluorophenyl)boronic acid
121219-16-7

(2,3-difluorophenyl)boronic acid

2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 100 percent / 10 percent aq. H2O2 / diethyl ether / 2.5 h / Heating
2: K2CO3 / acetone / 48 h / Heating
View Scheme
C12H17BF2O2

C12H17BF2O2

2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 100 percent / 10 percent aq. HCl / 1 h / 20 °C
2: 100 percent / 10 percent aq. H2O2 / diethyl ether / 2.5 h / Heating
3: K2CO3 / acetone / 48 h / Heating
View Scheme
1-Bromoheptane
629-04-9

1-Bromoheptane

2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

Conditions
ConditionsYield
With potassium carbonate48.5 g (89%)
acetyl chloride
75-36-5

acetyl chloride

2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2,3-difluoro-4-(heptyloxy)-acetophenone
122265-89-8

2,3-difluoro-4-(heptyloxy)-acetophenone

Conditions
ConditionsYield
With iron(III) chloride In dichloromethane Ambient temperature;47%
With iron(III) chloride In dichloromethane
Triisopropyl borate
5419-55-6

Triisopropyl borate

2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

C19H31BF2O3

C19H31BF2O3

Conditions
ConditionsYield
Stage #1: 2,3-difluoro-4-(heptyloxy)benzene With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 2.5h; Metallation;
Stage #2: Triisopropyl borate In tetrahydrofuran; hexane at -78 - 20℃; Substitution;
N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

4-Heptoxy-2,3-difluorobenzaldehyde

4-Heptoxy-2,3-difluorobenzaldehyde

Conditions
ConditionsYield
Stage #1: 2,3-difluoro-4-(heptyloxy)benzene With n-butyllithium In tetrahydrofuran; hexane at -78℃;
Stage #2: N,N-dimethyl-formamide In tetrahydrofuran; hexane at -78 - 20℃;
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2-(2,3-difluoro-4-heptyloxy-phenyl)-5-(4-pentyl-phenyl)-[1,3]dioxane

2-(2,3-difluoro-4-heptyloxy-phenyl)-5-(4-pentyl-phenyl)-[1,3]dioxane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: n-BuLi / hexane; tetrahydrofuran / -78 °C
1.2: hexane; tetrahydrofuran / -78 - 20 °C
2.1: p-toluenesulfonic acid / toluene / Heating
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2-(2,3-difluoro-4-heptyloxy-phenyl)-5-(2-fluoro-4-pentyl-phenyl)-[1,3]dioxane

2-(2,3-difluoro-4-heptyloxy-phenyl)-5-(2-fluoro-4-pentyl-phenyl)-[1,3]dioxane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: n-BuLi / hexane; tetrahydrofuran / -78 °C
1.2: hexane; tetrahydrofuran / -78 - 20 °C
2.1: p-toluenesulfonic acid / toluene / Heating
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2-(2,3-difluoro-4-heptyloxy-phenyl)-5-(4-heptyl-phenyl)-[1,3]dioxane

2-(2,3-difluoro-4-heptyloxy-phenyl)-5-(4-heptyl-phenyl)-[1,3]dioxane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: n-BuLi / hexane; tetrahydrofuran / -78 °C
1.2: hexane; tetrahydrofuran / -78 - 20 °C
2.1: p-toluenesulfonic acid / toluene / Heating
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2-(2,3-difluoro-4-heptyloxy-phenyl)-5-(4-nonyl-phenyl)-[1,3]dioxane

2-(2,3-difluoro-4-heptyloxy-phenyl)-5-(4-nonyl-phenyl)-[1,3]dioxane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: n-BuLi / hexane; tetrahydrofuran / -78 °C
1.2: hexane; tetrahydrofuran / -78 - 20 °C
2.1: p-toluenesulfonic acid / toluene / Heating
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2-(2,3-difluoro-4-heptyloxy-phenyl)-5-(2,3-difluoro-4-pentyl-phenyl)-[1,3]dioxane

2-(2,3-difluoro-4-heptyloxy-phenyl)-5-(2,3-difluoro-4-pentyl-phenyl)-[1,3]dioxane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: n-BuLi / hexane; tetrahydrofuran / -78 °C
1.2: hexane; tetrahydrofuran / -78 - 20 °C
2.1: p-toluenesulfonic acid / toluene / Heating
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2,3-difluoro-4-(heptyloxy)benzoic acid
122265-95-6

2,3-difluoro-4-(heptyloxy)benzoic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: FeCl3 / CH2Cl2
2: Br2; aq. NaOH / dioxane
View Scheme
Multi-step reaction with 2 steps
1: 47 percent / FeCl3 / CH2Cl2 / Ambient temperature
2: 54 percent / Br2 / aq. NaOH; dioxane / 1.) rt, 30 min; 2.) 50 deg C, 30 min
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

C48H48F4N2O6

C48H48F4N2O6

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: FeCl3 / CH2Cl2
2: Br2; aq. NaOH / dioxane
3: DCC; DMAP / CH2Cl2 / 20 °C
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2,3-Difluoro-4-n-heptoxyphenylboronic acid
147222-88-6

2,3-Difluoro-4-n-heptoxyphenylboronic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: n-butyllithium / hexane; tetrahydrofuran / 2.5 h / -78 °C
1.2: hexane; tetrahydrofuran / -78 - 20 °C
2.1: 10 percent aq. HCl / 1 h / 20 °C
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2-(2',3'-difluoro-4'-heptyloxy-biphenyl-4-yl)-5-pentyl-[1,3]dioxane

2-(2',3'-difluoro-4'-heptyloxy-biphenyl-4-yl)-5-pentyl-[1,3]dioxane

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: n-butyllithium / hexane; tetrahydrofuran / 2.5 h / -78 °C
1.2: hexane; tetrahydrofuran / -78 - 20 °C
2.1: 10 percent aq. HCl / 1 h / 20 °C
3.1: tetrakis(triphenylphosphine)palladium(0); aq. Na2CO3 / 1,2-dimethoxy-ethane / 24 h / Heating
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2-(2',3'-difluoro-4'-heptyloxy-biphenyl-4-yl)-5-hexyl-[1,3]dioxane

2-(2',3'-difluoro-4'-heptyloxy-biphenyl-4-yl)-5-hexyl-[1,3]dioxane

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: n-butyllithium / hexane; tetrahydrofuran / 2.5 h / -78 °C
1.2: hexane; tetrahydrofuran / -78 - 20 °C
2.1: 10 percent aq. HCl / 1 h / 20 °C
3.1: tetrakis(triphenylphosphine)palladium(0); aq. Na2CO3 / 1,2-dimethoxy-ethane / 24 h / Heating
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2-(2',3'-difluoro-4'-heptyloxy-biphenyl-4-yl)-5-heptyl-[1,3]dioxane

2-(2',3'-difluoro-4'-heptyloxy-biphenyl-4-yl)-5-heptyl-[1,3]dioxane

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: n-butyllithium / hexane; tetrahydrofuran / 2.5 h / -78 °C
1.2: hexane; tetrahydrofuran / -78 - 20 °C
2.1: 10 percent aq. HCl / 1 h / 20 °C
3.1: tetrakis(triphenylphosphine)palladium(0); aq. Na2CO3 / 1,2-dimethoxy-ethane / 24 h / Heating
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2-(2',3'-difluoro-4'-heptyloxy-biphenyl-4-yl)-5-octyl-[1,3]dioxane

2-(2',3'-difluoro-4'-heptyloxy-biphenyl-4-yl)-5-octyl-[1,3]dioxane

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: n-butyllithium / hexane; tetrahydrofuran / 2.5 h / -78 °C
1.2: hexane; tetrahydrofuran / -78 - 20 °C
2.1: 10 percent aq. HCl / 1 h / 20 °C
3.1: tetrakis(triphenylphosphine)palladium(0); aq. Na2CO3 / 1,2-dimethoxy-ethane / 24 h / Heating
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2-(2',3'-difluoro-4'-heptyloxy-biphenyl-4-yl)-5-nonyl-[1,3]dioxane

2-(2',3'-difluoro-4'-heptyloxy-biphenyl-4-yl)-5-nonyl-[1,3]dioxane

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: n-butyllithium / hexane; tetrahydrofuran / 2.5 h / -78 °C
1.2: hexane; tetrahydrofuran / -78 - 20 °C
2.1: 10 percent aq. HCl / 1 h / 20 °C
3.1: tetrakis(triphenylphosphine)palladium(0); aq. Na2CO3 / 1,2-dimethoxy-ethane / 24 h / Heating
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2,3-Difluoro-4-heptyloxy-benzoic acid 4-[2-(4-propyl-cyclohexyl)-ethyl]-phenyl ester

2,3-Difluoro-4-heptyloxy-benzoic acid 4-[2-(4-propyl-cyclohexyl)-ethyl]-phenyl ester

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 47 percent / FeCl3 / CH2Cl2 / Ambient temperature
2: 54 percent / Br2 / aq. NaOH; dioxane / 1.) rt, 30 min; 2.) 50 deg C, 30 min
3: dicyclohexyl carbodiimide / 4-dimethylaminopyridine / CH2Cl2 / Ambient temperature
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2,3-Difluoro-4-heptyloxy-benzoic acid 4-[2-(4-pentyl-cyclohexyl)-ethyl]-phenyl ester

2,3-Difluoro-4-heptyloxy-benzoic acid 4-[2-(4-pentyl-cyclohexyl)-ethyl]-phenyl ester

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 47 percent / FeCl3 / CH2Cl2 / Ambient temperature
2: 54 percent / Br2 / aq. NaOH; dioxane / 1.) rt, 30 min; 2.) 50 deg C, 30 min
3: dicyclohexyl carbodiimide / 4-dimethylaminopyridine / CH2Cl2 / Ambient temperature
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2,3-Difluoro-4-heptyloxy-benzoic acid 4-{2-[((E)-4-pent-1-enyl)-cyclohexyl]-ethyl}-phenyl ester

2,3-Difluoro-4-heptyloxy-benzoic acid 4-{2-[((E)-4-pent-1-enyl)-cyclohexyl]-ethyl}-phenyl ester

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 47 percent / FeCl3 / CH2Cl2 / Ambient temperature
2: 54 percent / Br2 / aq. NaOH; dioxane / 1.) rt, 30 min; 2.) 50 deg C, 30 min
3: dicyclohexyl carbodiimide / 4-dimethylaminopyridine / CH2Cl2 / Ambient temperature
View Scheme
2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2,3-Difluoro-4-heptyloxy-benzoic acid 4-[2-(4-heptyl-cyclohexyl)-ethyl]-phenyl ester

2,3-Difluoro-4-heptyloxy-benzoic acid 4-[2-(4-heptyl-cyclohexyl)-ethyl]-phenyl ester

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 47 percent / FeCl3 / CH2Cl2 / Ambient temperature
2: 54 percent / Br2 / aq. NaOH; dioxane / 1.) rt, 30 min; 2.) 50 deg C, 30 min
3: dicyclohexyl carbodiimide / 4-dimethylaminopyridine / CH2Cl2 / Ambient temperature
View Scheme
Trimethyl borate
121-43-7

Trimethyl borate

2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

2,3-difluoro-4-n-heptyloxyphenyl boric acid

2,3-difluoro-4-n-heptyloxyphenyl boric acid

Conditions
ConditionsYield
With n-butyllithium In tetrahydrofuran; hexane

122265-84-3Relevant articles and documents

COMPOUNDS FOR USE IN LIQUID CRYSTAL DEVICES

-

Page/Page column 27, (2008/06/13)

Liquid crystal compounds of Formula (I) for use in liquid crystal devices contains a dioxatetralin unit within the mesogenic liquid crystal core. The dioxatetralin unit may be located at any position within the mesogenic core of the liquid crystal compound, either at the terminus of the liquid crystal core or alternatively substantially in the middle of the liquid crystal core. The compounds of the invention exhibit fast switching and may be used in liquid crystal mixtures for particular use in imaging or display media, such as monitors or televisions.

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.

The synthesis and electro-optic properties of liquid crystalline 2- (2,3-difluorobiphenyl-4'-yl)-1,3-dioxanes

Dong, Chu Chuan,Styring, Peter,Goodby, John W.,Chan, Lawrence K. M.

, p. 1669 - 1677 (2007/10/03)

Fifty-six novel alkyl and/or alkoxy disubstituted 2-(2,3- difluorobiphenyl-4'-yl)-1,3-dioxanes (DFBPD) were prepared. Smectic C and nematic mesophases were exhibited by most of the alkyl-alkoxy homologues. Conversely, most of the dialkyl compounds exhibited smectic C, smectic A and nematic phases. The birefringence (Δn), dielectric anisotropy (Δε), spontaneous polarisation and response times of two ferroelectric mixtures formulated from the dioxanyl systems were determined. The birefringence results were compared with eight other groups of mixtures where the materials were based on different core systems. The overall electro-optic properties of the DFBPDs were found to be comparable to the best of the eight most commonly used materials in ferroelectric display devices.

Dioxane derivatives

-

, (2008/06/13)

Dioxane derivatives for use as components in liquid crystal devices (LCDs) of general formula (A), wherein X is CH or B; R1, R2 are each A1, OA1, OCOA2, or COOA2 ; A1 is a straight or branched chain alkyl group containing from 1 to 20 carbon atoms and may be substituted with one or more F or CN. A2 is a straight or branched chain alkyl group containing from 1 to 20 carbon atoms and may be substituted with one or more F or CN and if straight may be unsubstituted. Y1, Y2, Y3 may each be (CH2)p, (CH2)p COO or OCO(CH2)p ; p is from 0 to 10, n is 0 or 1, m is 0 or 1, either or both of Z1 and Z2 are F and, when not F, are H; Y4 is a covalent bond or, when n is 0, may be (a) LCDs, containing the devices exhibit very fast switching speed, bi-stable characteristics, enhanced greyscale and storage capabilities and a wide viewing angle.

Liquid crystal compounds and compositions

-

, (2008/06/13)

Liquid crystal naphtalene compounds, represented by the following formula (1) are disclosed. R-Z-A-NAP-Z?-R? (1)In the formula (1), R is an alkyl group containing 1 to 18 carbon atoms; R? is an alkyl group containing 1 to 21 carbon atoms; NAP represents 2,6-naphthylene group; A, Z and Z? are as follows: 1) A is Pyr> and (a) Z is - or and Z? is O, or (b) Z is - and Z? is COO; 2) if A is Pym>, (a) Z is - and Z? is O, or (b) Z is O and Z? is -, O or ; 3) A is FPhF and (a) Z is - or O and Z? is -, O or COO, (b) Z is OCO and Z? is - or O, or (c) Z is and Z? is O; 4) A is PhF and (a) Z is - or and Z? is O, (b) Z is O and Z? is -, or (c) Z is - and Z? is COO; 5) A is FPh and (a) Z is O and Z? is-, (b) Z is -, O, or OCO and Z? is O, or (c) Z is O and Z? is COO; 6) A is Pyr and Z is -, O or and Z? is O; or 7) A is Ph and one of Z and Z? is - and the other is O; As a component of liquid crystal compositions showing chiral smectic C phase, these compounds can provide liquid crystal compositions of improved orientation and free from zigzag deffects, and liquid crystal display elements of high contrast ratio.

67. Ferroelectric Liquid Crystals. Laterally Substituted Phenyl Benzoates Incorporating a trans-1,4-Disubstituted Cyclohexane Ring.

Kelly, Stephen M.

, p. 594 - 607 (2007/10/02)

About 65 diverse phenyl benzoates incorporating a trans-1,4-disubstituted cyclohexane ring and at least one lateral substituent have been synthesised.The dependence of the liquid-crystal transition temperatures of these materials on various lateral substituents (F, Cl, CN, and Br) in different positions of the esters has been investigated systematically.The influence of up to four F-atoms in various positions of a standard ester has been thoroughly studied and the optimum combination for a broad smectic C mesomorphic range established.In consequence, three homologous series incorporating the 4-alkoxy-2,3-difluorobenzoic-acid moiety were prepared.An additional C=C bond was introduced into the alkyl chain attached to the cyclohexane ring of some of these esters and the resulting modifications of the transition temperatures determined.Three ester series incorporating a lateral substituent and the optically active (+)-(S)-(1-methylphenyl)oxy substituent have also been synthesised, and similar effects have been observed.These materials can be used as important components of commercial chiral smectic C mixtures for electro-optic display device applications.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 122265-84-3