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78531-61-0

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78531-61-0 Usage

Chemical Properties

White solid

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 78531-61-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,3 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 78531-61:
(7*7)+(6*8)+(5*5)+(4*3)+(3*1)+(2*6)+(1*1)=150
150 % 10 = 0
So 78531-61-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H24O/c1-3-4-14-5-7-16(8-6-14)17-11-9-15(10-12-17)13(2)18/h9-12,14,16H,3-8H2,1-2H3/t14-,16-

78531-61-0SDS

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 1-phenyl-2-(4-propylcyclohexyl)ethanone

1.2 Other means of identification

Product number -
Other names TRANS-4-PROPYL CYCLOHEXYL ACETOPHENONE

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:78531-61-0 SDS

78531-61-0Relevant articles and documents

SYNTHESIS AND SOME PROPERTIES OF NEMATIC COMPOUNDS CONTAINING THREE RING SYSTEMS.

Takatsu,Takeuchi,Sato

, p. 311 - 319 (2007/10/02)

Four series of nematic compounds were prepared and their transition temperatures and transition entropies measured. Their flow-aligned viscosities and birefringences were determined by extrapolation. 7 refs.

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.

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