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17408-60-5

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17408-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17408-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,0 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17408-60:
(7*1)+(6*7)+(5*4)+(4*0)+(3*8)+(2*6)+(1*0)=105
105 % 10 = 5
So 17408-60-5 is a valid CAS Registry Number.

17408-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-decan-3-ylphenol

1.2 Other means of identification

Product number -
Other names p-1-ethyloctylphenol

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:17408-60-5 SDS

17408-60-5Relevant articles and documents

Alkylation of Phenol by 1-Dodecene and 1-Decanol. A Literature Correction

Campbell, Curt B.,Onopchenko, Anatoli,Santilli, Donald S.

, p. 3665 - 3669 (2007/10/02)

A recent literature report that 1-dodecene reacts with phenol in the presence of sulfated zirconium oxide (superacid), or 1-dodecanol with phenol in the presence of H-Mordenite (zeolite), to afford mostly para-substituted alkylphenols has been shown to be incorrect.The product with zirconium is a mixture of ortho/para isomers (ca. 50-65/50-35), and not the exclusive para isomer as reported.The major product in the case of zeolite catalysis is the o-alkylphenol, with a high degree of end attachment, and not the predominantly claimed para isomers.The selectivity obtained with H-Mordenite during alkylation of phenol differs from the a lkylation of alkylbenzenes and anisole, and is best explained on the basis of a surface catalysis phenomenon.

EQUILIBRIUM OF POSITIONAL ISOMERIZATION OF SECONDARY ALKYLBENZENES AND THEIR FUNCTIONAL DERIVATIVES

Nasterova, T. N.,Roshchupkina, I. Yu.,Pimerzin, A. A.

, p. 1445 - 1449 (2007/10/02)

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