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1-Hexanol, 6-cyclohexylidene- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111998-14-2

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111998-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111998-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,9,9 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 111998-14:
(8*1)+(7*1)+(6*1)+(5*9)+(4*9)+(3*8)+(2*1)+(1*4)=132
132 % 10 = 2
So 111998-14-2 is a valid CAS Registry Number.

111998-14-2SDS

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 6-cyclohexylidene-1-hexanol

1.2 Other means of identification

Product number -
Other names 6-cyclohexylidene-hexan-1-ol

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:111998-14-2 SDS

111998-14-2Relevant academic research and scientific papers

Chain-modified pyridino-N substituted nicotine compounds for use in the treatment of CNS pathologies

-

Page 10, (2010/02/05)

Compounds for treating abuse of nicotinic receptor agonists, addiction to psychostimulant drugs, addiction to opiates, addiction to alcohol, addiction to tobacco products, addiction to nicotine, schizophrenia and related diseases, depression and related conditions, Alzheimer's disease, Parkinson's disease, irritable bowel syndrome, and colitis. The compounds competitively inhibit central nervous system acting nicotinic receptor agonists and act at the putative α3β2* and α4β2 neuronal nicotinic receptors in the central nervous system.

Inter- and Intramolecular hetero Diels-Alder Reactions, XXI - Intramolecular hetero Diels-Alder Reaction of Alkylidene-1,3-dicarbonyl Compounds. Experimental Evidence for an Asymmetric Transition State

Tietze, Lutz F.,Brumby, Thomas,Brand, Siegbert,Bratz, Matthias

, p. 499 - 506 (2007/10/02)

The intramolecular hetero Diels-Alder reaction of heterodienes 13 is described.The heterodienes, which are obtained in situ by Knoevenagel condensation of aldehydes 12a-e with dimethylbarbituric acid (2), yield the cycloadducts 14a-e/15a-e and the ene adducts 16a, c-e/17a, c-e.The ratio of 14/15 was determined by HPLC.The resulting data are interpreted as experimental evidence of an asymmetrical transition state of the Diels-Alder reaction.

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