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Cyclohexanone, 4-(1,1-dimethylethyl)-3-ethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100103-31-9

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100103-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100103-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,0 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 100103-31:
(8*1)+(7*0)+(6*0)+(5*1)+(4*0)+(3*3)+(2*3)+(1*1)=29
29 % 10 = 9
So 100103-31-9 is a valid CAS Registry Number.

100103-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-tert-Butyl-3-ethylcyclohexanone

1.2 Other means of identification

Product number -
Other names 4-tert-Butyl-3-ethyl-cyclohexanone

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:100103-31-9 SDS

100103-31-9Upstream product

100103-31-9Downstream Products

100103-31-9Relevant academic research and scientific papers

COMPOUNDS FOR INHIBITING KSP KINESIN ACTIVITY

-

Page/Page column 177, (2010/11/23)

The present invention provides compounds of Formula (I) (wherein R1, R3, X, W, Z and ring Y are as defined herein). The present invention also provides compositions comprising these compounds that are useful for treating cellular proliferative diseases or disorders associated with KSP kinesin activity and for inhibiting KSP kinesin activity.

1,4-Addition of Triorganozincates and Silyldiorganozincates to α,β-Unsaturated Ketones

Tueckmantel, Werner,Oshima, Koichiro,Nozaki, Hitosi

, p. 1581 - 1593 (2007/10/02)

Lithium and magnesium triorganozincates, prepared by combination of ZnCl2(TMEDA) with 3 molar equivalents of RLi or RMgX, or from dialkylzinc and 1 molar equivalent of RLi or RMgX, react with 2-cyclohexen-1-one (1) under mild conditions to produce moderate to good yields of the 1,4-addition products 2.The approximate reactivity order obtained from the product distribution using unsymmetrical zincates is tBuCH2 tBu, Me Me2PhSi.The latter groups are transferred with good selectivity from mixed reagents derived from Me2Zn.This sequence differs strikingly from that exhibited by unsymmetrical cuprates which transfer neopentyl very easily, and also tert-butyl more easily than the corresponding zincates.The methylation with Me3ZnLi is catalyzed by cobalt complexes.Other enones (7-13) generally give poor yields, and the cobalt-catalyzed methylation of isophorone (3) is complicated by a Kharasch-type deconjugation.Mixed silyldialkylzincates, Me2PhSiZnR2Li, produce the β-silyl ketones from a variety of unhindered or moderately hindered enones in practically useful yields; one example of an α,β-unsaturated ester (12) is also included.

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