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147222-99-9

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147222-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147222-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,2 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 147222-99:
(8*1)+(7*4)+(6*7)+(5*2)+(4*2)+(3*2)+(2*9)+(1*9)=129
129 % 10 = 9
So 147222-99-9 is a valid CAS Registry Number.

147222-99-9SDS

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 (4-decoxyphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 4-decyloxyphenyboronic acid

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:147222-99-9 SDS

147222-99-9Relevant articles and documents

Ferro-, ferri- and antiferro-electric behaviour in a bent-shaped mesogen

Matharu, Avtar S.,Grover, Chrissie,Komitov, Lachezar,Andersson, Gunnar

, p. 1303 - 1310 (2000)

The synthesis of a novel bent-shaped, four-ring thiophene-based chiral liquid crystalline ester derived from 5-(4-n-decyloxyphenyl)thiophene-2- carboxylic acid and (S)-1-methylheptyl 4'-hydroxybiphenyl-4-carboxylate is reported, i.e., (S)-4'-(1-methylheptyloxycarbonyl)biphenyl-4-yl 5-(4-n- decyloxyphenyl)thiophene-2-carboxylate. Optical microscopy, differential scanning calorimetry, miscibility study, and complementary electro-optical and current response studies reveal the existence of the SmA*, SmC* ferroelectric, SmC* ferrielectric, SmC* antiferroelectric and SmI* antiferroelectric phase types. Another mesophase type possibly exists below SmI* antiferroelectric which generates a rapid electro-optic response. Comparison with the analogous three-ring compound, i.e., (S)-4-(1- methylheptyloxycarbonyl)phenyl 5-(4-n-decyloxyphenyl)thiophene-2-carboxylate increases the thermal stability by 95.8 °C and the SmI* antiferroelectric phase is observed in addition.

New pyridine based liquid crystalline esters with different terminal chains

Karanl?k, Gürkan,Ocak, Hale,Bilgin Eran, Belk?z

, (2019/08/22)

The synthesis, structural and mesomorphic characterization of new pyridine-based methyl esters carrying a n-alkoxy chain or 3,7-Dimethyloctyloxy branched group at terminal have been presented. The liquid crystalline properties of the new pyridine-based calamitic molecules have been investigated by polarized optical microscopy and differential scanning calorimetry. New compounds exhibit enantiotropic smectic A mesophase at a variable mesomorphic range depending on alkoxy chain length and branching at terminal. The presence of a branched terminal group in chiral or racemic form gives rise to a sharply increase in mesomorphic range as well as decrease in crystallization points by preserving mesophase type.

Arylation of chloroanthraquinones by surprisingly facile Suzuki-Miyaura cross-coupling reactions

Thiemann, Thies,Tanaka, Yasuko,Iniesta, Jesus,Varghese, H. Tresa,Pannicker, C. Yohannan

experimental part, p. 732 - 736 (2010/03/24)

Chloroanthraquinones were found to undergo facile Suzuki-cross coupling with substituted phenyl boronic acids using a commercial catalyst Pd(PPh 3)4 and with Pd(PPh3)4 prepared in situ from Pd(PPh3)2Cl2 and PPh3.

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