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Benzene, (4-heptylcyclohexyl)-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61203-98-3

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61203-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61203-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,0 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61203-98:
(7*6)+(6*1)+(5*2)+(4*0)+(3*3)+(2*9)+(1*8)=93
93 % 10 = 3
So 61203-98-3 is a valid CAS Registry Number.

61203-98-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-1-heptyl-4-phenylcyclohexane

1.2 Other means of identification

Product number -
Other names trans-4-heptyl-1-phenylcyclohexane

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:61203-98-3 SDS

61203-98-3Relevant academic research and scientific papers

Synthesis and Liquid Crystalline Properties of 1-(trans-4-Alkylcyclohexylethyl)-4-Alkyl- and -4-Alkoxy-Benzenes, Their Ketone Precursors, and Some Lateral Fluoro-Derivatives

Gray, George W.,Lacey, David,Scrowston, Richard M.,Shenouda, Ibrahim G.,Toyne, Kenneth J.

, p. 101 - 116 (2007/10/02)

The preparation of some 1-(trans-4-alkylcyclohexylethyl)-4-alkyl- and -4-alkoxy-benzenes, their methylenecarbonyl linked analogues and their laterally fluoro- and bromo-substituted derivatives is reported.Twenty-four inter-related compounds have been prepared and the trends in their transition temperatures are discussed.Both the melting points and clearing points for these compounds are relatively low and, in general, SB and SA phases predominate.The suitability of these compounds as additives to SC materials has been assessed using two SC hosts.Keywords: Mesogenic cyclohexylethanes, mesogenic ketones, fuoro-substitution of mesogens

SYNTHESIS OF TRANS-4-ALKYL-1-PHENYLCYCLOHEXANES AND THEIR DERIVATIVES

Bezborodov, V. S.,Bubel', O. N.,Konovalov, V. A.,Ptashnikov, Yu. L.

, p. 1479 - 1483 (2007/10/02)

The alkylation of benzene by 1-alkanoyl-2-chlorocyclohexanes and 1-alkanoyl-1-cyclohexenes leads to the formation of cis- and trans-4-alkanoyl-1-phenylcyclohexanes, the yields of which increase with increase in the reaction temperature. trans-4-Alkyl-1-phenylcyclohexanes were obtained from 4-alkanoyl-1-phenylcyclohexanes and also from the products from the reaction of 4-alkylcyclohexanones with phenylmagnesium bromide.Some mesomorphous derivatives of these hydrocarbons were synthesized.

CONVENIENT SYNTHESIS OF 4-(TRANS-4 prime -N-ALKYLCYCLOHEXYL) BENZOIC ACIDS.

Szczucinski,Dabrowski

, p. 55 - 64 (2007/10/02)

A convenient method of obtaining 4-(trans-4 prime -n-alkylcyclohexyl) benzoic acids from alkanoyl chlorides, cyclohexane and benzene is described. Homologous series of above mentioned acids and their nitriles with alkyl tail 2 to 10 carbon atoms were prepared and temperatures of their phase transitions were determined.

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