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36823-84-4

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36823-84-4 Usage

Chemical Properties

clear colorless to light yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 36823-84-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,2 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 36823-84:
(7*3)+(6*6)+(5*8)+(4*2)+(3*3)+(2*8)+(1*4)=134
134 % 10 = 4
So 36823-84-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H15ClO2/c1-2-3-4-9-15-11-7-5-10(6-8-11)12(13)14/h5-8H,2-4,9H2,1H3

36823-84-4 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (A15019)  4-n-Pentyloxybenzoyl chloride, 97%   

  • 36823-84-4

  • 1g

  • 153.0CNY

  • Detail
  • Alfa Aesar

  • (A15019)  4-n-Pentyloxybenzoyl chloride, 97%   

  • 36823-84-4

  • 5g

  • 484.0CNY

  • Detail
  • Alfa Aesar

  • (A15019)  4-n-Pentyloxybenzoyl chloride, 97%   

  • 36823-84-4

  • 25g

  • 2156.0CNY

  • Detail

36823-84-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-N-PENTYLOXYBENZOYL CHLORIDE

1.2 Other means of identification

Product number -
Other names Benzoyl chloride, 4-(pentyloxy)-

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:36823-84-4 SDS

36823-84-4Relevant articles and documents

Synthesis of new liquid-crystalline compounds from the 3-aryl-5- alkylpyrazole series

Kovganko,Kovganko

, p. 696 - 700 (2006)

A method was developed for the preparation of new liquid-crystalline substances, pyrazole derivatives, through the corresponding 2-isoxazolines and isoxazoles. The hydrogenolysis of the heterocycle in 3-(4-hydroxyphenyl)-5- amylisoxazole afforded 1-amino-1-(4-hydroxyphenyl)-1-octen-3-one. The acid hydrolysis of the compound followed by treating with hydrazine hydrate resulted in 5-amyl-3-(4-hydroxyphenyl)-1H-pyrazole, whose benzylation and esterification with the corresponding mesogenous benzyl chlorides and benzoyl chlorides provided liquid-crystalline 5-alkyl-3-aryl-1H-pyrazoles. Pleiades Publishing, Inc. 2006.

Dependence of mesomorphism on terminal polar group in novel azoester series

Kher, Seema N.,Prajapati,Makwana,Chandra, Raviprakash S.

, p. 44 - 53 (2019/10/14)

Novel homologous series 4-(4′-n-alkoxy benzoyloxy) napthyl azo 4″–bromo benzenes, consisted of 11 members of a series. All the 11 members (ethoxy to hexadecyloxy) except hexadecyloxy are only enantiotropically nematogenic without exhibition of any smectogenic character. Transition temperatures and the textures are determined by an optical polarizing microscopy equipped with a heating stage. Textures of a nematic phase are threaded or schlieren. Analytical and spectral data supported the molecular structure of homologs. Transition curves viz., solid-nematic and nematic-isotropic showing phase behavior of the mesophase in a phase diagram behave in normal manner. Alternation of transition temperatures is exhibited by N–I transition curve. Thus, novel series is entirely nematogenic and high ordered melting type. Thus, synthesis of a novel azoester homologous series is carried out with a view to understand and establish the effect of molecular structure on Liquid crystal (LC) behaviors of a substance.

Study of Y-shaped liquid crystalline materials with polar nitro substituent

Dixit, Sandhya

, p. 77 - 84 (2018/06/27)

A new homologous series of Y-shaped liquid crystals namely 4-Nitro-[2′4′bis (4″-n-alkoxybenzoyloxy)] phenyl bisazobenzenes have been synthesized and its thermotropic properties studied on the hot stage of a polarizing microscope. The compounds consist four phenyl rings joined through ester and bisazo linkages with alkoxy and nitro as terminal substituents. The structures of synthesized compounds were confirmed by spectroscopic techniques such as FTIR, 1HNMR as well as elemental analysis. The compounds were found to exhibit enantiotropic nematic and smectic mesophases. The role of molecular shape, size and polarity of functional groups in the mesophases formation is discussed.

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