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6850-63-1

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6850-63-1 Usage

General Description

2,6-Dimethylcyclohexylamine is a chemical compound with the molecular formula C8H17N. It is an amine derivative, specifically a cyclohexylamine, and is composed of a cyclohexane ring with two methyl groups and an amine functional group. 2,6-DIMETHYLCYCLOHEXYLAMINE is used in various industrial applications, including as an intermediate in the manufacturing of pharmaceuticals and dyes. It is also used as a corrosion inhibitor in metalworking fluids and as a chemical intermediate in the production of rubber chemicals and surfactants. 2,6-Dimethylcyclohexylamine can be a hazardous material if not handled or stored properly, and exposure to it can cause irritation to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 6850-63-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,5 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6850-63:
(6*6)+(5*8)+(4*5)+(3*0)+(2*6)+(1*3)=111
111 % 10 = 1
So 6850-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H17N/c1-6-4-3-5-7(2)8(6)9/h6-8H,3-5,9H2,1-2H3

6850-63-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dimethylcyclohexan-1-amine

1.2 Other means of identification

Product number -
Other names 2,6-Dimethylcyclohexylamine

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:6850-63-1 SDS

6850-63-1Relevant articles and documents

SULPHONYL UREA DERIVATIVES AS NLRP3 INFLAMMASOME MODULATORS

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Paragraph 01072, (2019/07/13)

The present disclosure relates to compounds of Formula (I): (I) and to their pharmaceutically acceptable salts, pharmaceutical compositions, methods of use, and methods for their preparation. The compounds disclosed herein are useful for inhibiting the maturation of cytokines of the IL-1 family by inhibiting inflammasomes and may be used in the treatment of disorders in which inflammasome activity is implicated, such as inflammatory, autoinflammatory and autoimmune diseases and cancers.

N-substituted diphosphinoamines: Toward rational ligand design for the efficient tetramerization of ethylene

Kuhlmann, Sven,Blann, Kevin,Bollmann, Annette,Dixon, John T.,Killian, Esna,Maumela, Munaka C.,Maumela, Hulisani,Morgan, David H.,Pretorius, Marie,Taccardi, Nicola,Wasserscheid, Peter

, p. 279 - 284 (2007/10/03)

Bis(diphenylphosphino)amine (PNP) ligands with different alkyl and cycloalkyl substituents attached to the N atom of the ligand backbone were synthesised and tested together with chromium as ethylene tetramerization catalysts. On activation with a methylaluminoxane-based activator, the catalysts displayed good activity and selectivity toward 1-octene and 1-hexene, with the best ligand systems containing cyclopentyl or cyclohexyl moieties. In addition, it was established that substitution at the 2 position of the cyclohexyl skeleton and, more importantly, an increase in steric bulk at that point, led to a drastic reduction of side product formation (i.e., methyl- and methylenecyclopentane). Interestingly, additional methyl substitution in the 6 position of the cyclohexyl ring changed the selectivity of the catalyst from predominantly tetramerization to a 1:1 mixture of 1-hexene and 1-octene. Structurally similar ligands, such as cyclohexylmethyl and cyclohexylethyl PNP, were also tested and were also found to yield efficient tetramerization catalysts. It was concluded that structural fine tuning of the N-alkyl moiety of the PNP ligand is essential for obtaining efficient tetramerization catalysts, with the best systems achieving combined selectivities as high as 88% (1-octene and 1-hexene) with exceptionally high activities exceeding 2,000,000 g/(g-Cr h).

Chloroacetic acid cyclohexylamides, their preparation, their use for controlling weeds and agents for this use

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, (2008/06/13)

Novel chloroacetic acid cyclohexylamides of the formula I STR1 where R1, R2 and R3 have the meanings given in the description, their preparation and their use as herbicides.

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