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17385-32-9

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17385-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17385-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,8 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17385-32:
(7*1)+(6*7)+(5*3)+(4*8)+(3*5)+(2*3)+(1*2)=119
119 % 10 = 9
So 17385-32-9 is a valid CAS Registry Number.

17385-32-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclopent-2-en-1-ylcyclopentene

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:17385-32-9 SDS

17385-32-9Upstream product

17385-32-9Downstream Products

17385-32-9Relevant articles and documents

High selectivity of MCM-22 for cyclopentanol formation in liquid-phase cyclopentene hydration

Nuntasri, Duangamol,Wu, Peng,Tatsumi, Takashi

, p. 272 - 280 (2007/10/03)

Highly effective formation of cyclopentanol through the liquid-phase hydration of cyclopentene has been attempted on various zeolites catalysts. MCM-22 zeolite was the most selective catalyst, which actively converted cyclopentene to cyclopentanol with a selectivity up to 99%. The effects on the hydration of catalyst preparation method, reaction atmosphere and temperature have been investigated for the MCM-22 catalysts. On the basis of the effect of reaction atmosphere, the mechanism of liquid-phase cyclopentene hydration was proposed. The thermodynamic equilibrium between cyclopentene and cyclopentanol was suggested to control greatly the cyclopentene conversion. The cyclopentene conversion was increased to 10% by increasing the water/cyclopentene ratio. Poisoning using organic amines with different molecular sizes revealed that the hydration occurred mainly in the 10-membered ring channels of MWW structure, which had an elliptic aperture smaller than that of MFI structure, exhibiting a significant shape selectivity by suppressing the etherification cyclopentanol.

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