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Ethanone, 2-bromo-1-[4-(decyloxy)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64328-75-2

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64328-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64328-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,2 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64328-75:
(7*6)+(6*4)+(5*3)+(4*2)+(3*8)+(2*7)+(1*5)=132
132 % 10 = 2
So 64328-75-2 is a valid CAS Registry Number.

64328-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-1-(4-decoxyphenyl)ethanone

1.2 Other means of identification

Product number -
Other names -

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:64328-75-2 SDS

64328-75-2Upstream product

64328-75-2Relevant academic research and scientific papers

PHENACYL ESTERS - A NEW TYPE OF LUQUID-CRYSTALLINE COMPOUND

Torgova, S. I.,Karamysheva, L. A.,Agafonova, I. F.

, p. 1162 - 1168 (2007/10/02)

The reaction of aliphatic, alicyclic, and aromatic acids with 4-substituted α-bromoacetophenones gave a series of new liquid-crystalline phenacyl esters.Their mesomorphous characteristics are discussed in relation to the structures of the acid and ketone parts of the molecule.

LES TRIBROMURES DE PHOSPHONIUMS. AGENTS DE BROMINATION DE SUBSTRATS ORGANIQUES

Cristau, Henri-Jean,Torreilles, Eliane,Morand, Philippe,Christol, Henri

, p. 357 - 368 (2007/10/02)

The reactivities and selectivities of phosphonium tribromides 1-4 towards ketones and their ketals, in the presence of other functional group reactive toward bromide (free enolic position, activated aromatic ring or double bond), are studied and compared with the trimethyl phenyl ammonium tribromide 5.The abilities of the two kinds of tribromides are similar, with a better selectivity of phosphonium salts toward unsaturated ketones, which is probably induced by the greater stability of the ion-pair in phosphonium salts.They act essentially by the tribromide without specific bond interactions between phosphorus and heteroatom of the substrate.

Synthese de derives du tetrathiafulvalene a proprietes mesomorphogenes

Polycarpe, Catherine,Torreilles, Eliane,Giral, Louis,Babeau, Annick,Tinh, Nguyen-Hun,Gasparoux, Henri

, p. 1741 - 1745 (2007/10/02)

We report the synthesis of di(4-alkoxyphenyl)- and di(4-alkanoyloxyphenyl)tetrathiafulvalenes.Their polymorphism has been investigated.

Transitions de Phase en Series Mesogenes: Les di TTF et les diTTF

Chann, N. B.,Cotrait, M.,Gautlier, J.,Haget, Y.,Tinh, Nguyen Huu,et al.

, p. 129 - 142 (2007/10/02)

The polymorphism of the di(4-alkylphenyl) and di(4-alkoxyphenyl) tetrathiafulvalene (TTF) is investigated by optical, crystallographic and calorimetric methods.All the studied derivatives are mesomorphic.The first mesophase is always a smectic G phase; th

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