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Benzoic acid, 4-hydroxy-, 1-methylheptyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

117599-73-2

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117599-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117599-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,5,9 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 117599-73:
(8*1)+(7*1)+(6*7)+(5*5)+(4*9)+(3*9)+(2*7)+(1*3)=162
162 % 10 = 2
So 117599-73-2 is a valid CAS Registry Number.

117599-73-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-1-(1-methylheptyloxycarbonyl)benzene

1.2 Other means of identification

Product number -
Other names 1-methylheptyl 4-hydroxybenzoate

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:117599-73-2 SDS

117599-73-2Relevant academic research and scientific papers

A chiral electrooptic response in a racemic liquid crystal

Cowling, Stephen J.,Hall, Alan W.,Goodby, John W.

, p. 1546 - 1548 (2007/10/03)

Over recent years, little attention has been paid to the electrooptic properties of racemic modifications of smectic liquid crystals, however, in this communication we report on a chiral response of a racemic modification to an applied electrical field wh

Two-rings-containing phenyl ester compound and anti-perroelectric liquid crystal composition containing the same

-

, (2008/06/13)

A two-rings-containing phenyl ester compound of the following general formula (1), wherein R1 is a linear alkyl group having 5 to 12 carbon atoms, R2 is a linear alkyl group having 1 to 15 carbon atoms, X1 and X2 are both hydrogen atoms or one of X1 and X2 is a fluorine atom and the other is a hydrogen atom, Y1 and Y2 are both hydrogen atoms or one of Y1 and Y2 is a fluorine atom and the other is a hydrogen atom, and A1 is a hydrogen atom, -CH3 or -CF3, provided that when A1 is a hydrogen atom or -CH3, p is 0 and that when A1 is -CF3, p is 1 and q is an integer of 5 to 8, and an anti-ferroelectric liquid crystal composition containing at least one of two-rings-containing phenyl ester compounds of the above general formula (1) in claim 1 and either an anti-ferroelectric liquid crystal compound or a mixture of anti-ferroelectric liquid crystal compounds.

Racemic compound and anti-ferroelectric liquid crystal composition

-

, (2008/06/13)

A racemic compound of the formula (1) and an anti-ferroelectric liquid crystal composition consisting essentially of said racemic compound and one anti-ferroelectric liquid crystal compound of the formula (2) or a mixture of two or more compounds selected

Process for the production of phenol derivatives

-

, (2008/06/13)

A process for the production of a phenol derivative of the formula (2), which comprises subjecting a diester compound of the formula (1) in which a hydroxyl group is protected by an acyl group, to a reaction for removal of protection, wherein the reaction is carried out in the presence of an aliphatic amine as a protection-removal agent, STR1 wherein X is hydrogen or fluorine, Y is --CH3 or --CF3, Q is an alkyl group having 1 to 4 carbon atoms, p is 0 or 1, m is an integer of 2 to 7, n is an integer of at least 1, and C* is an asymmetric carbon, the process enabling to obtain the phenol derivative of the formula (2) useful as an intermediate for a liquid crystal compound with ease and at high purity.

Liquid crystal compound

-

, (2008/06/13)

A liquid crystal compound represented by formula (I): STR1 wherein R1 represents an alkyl group having from 5 to 18 carbon atoms; R2 represents an alkyl group having from 4 to 15 carbon atoms; X represents a single bond, --O--, STR2

Liquid crystal compound

-

, (2008/06/13)

A new tetrastable liquid crystal is provided which is useful for display and switching devices. The liquid crystal has the formula STR1 where R1 is a C5-18 alkyl group and R2 is a C4-15 alkyl group and * is an o

Liquid crystal carbonatobenzoic acid derivative and composition

-

, (2008/06/13)

An optically active liquid crystal compound having a large spontaneous polarization value and a chiral smectic liquid crystal composition containing the same are provided, which compound is expressed by the formula STR1 wherein R1 and R2/

Synthesis and Physical Evaluation of Novel Ferroelectric Materials with High Spontaneous Polarization

Bone, M. F.,Bradshaw, M. J.,Chan, L. K. M.,Coates, D.,Constant, J.,et al.

, p. 117 - 134 (2007/10/02)

A large number of ferroelectric dopants incorporating a chiral lactate unit, -OC*H(CH3)CO2-, have been synthesized and extrapolated values of Ps as high as 160 nC cm-2 have been found, although many of these compounds did not show any liquid crystal behavior.Terphenyls and laterally fluoro-substitued terphenyls incorporating the chiral lactate unit have also been synthesized, and in one case, a ferroelectric host material with an S*C phase and a Ps value of 124 nC cm-2 was obtained.Compounds containing two chiral units (one of which was a chiral lactate unit) were also synthesized in which the two chiral units were either directly linked or separated by a phenyl ring; the latter compounds gave very high Ps values (199 nC cm-2).The effect of molecular structure on Ps, tilt angle and phase behavior is discussed for both the mono-lactates and the di-chiral compounds.An outline (with references) of the experimental procedures used to prepare these compounds is also given.

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