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Cyclohexanol, 4-(trimethylsilyl)-, cis- is a chemical compound with the molecular formula C9H22OSi. It is a derivative of cyclohexanol, where a trimethylsilyl group (Si(CH3)3) is attached to the 4-position of the cyclohexane ring. The cis-isomer indicates that the hydroxyl group (-OH) and the trimethylsilyl group are on the same side of the ring. Cyclohexanol, 4-(trimethylsilyl)-, cis- is an organosilicon compound, which is a type of compound that contains silicon and carbon atoms bonded together. It is used in various applications, such as in the synthesis of other organic compounds and as a reagent in chemical reactions. Due to its unique structure, it may exhibit different chemical properties compared to its parent compound, cyclohexanol.

7450-05-7

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7450-05-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7450-05-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,5 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7450-05:
(6*7)+(5*4)+(4*5)+(3*0)+(2*0)+(1*5)=87
87 % 10 = 7
So 7450-05-7 is a valid CAS Registry Number.

7450-05-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-4-(trimethylsilyl)cyclohexanol

1.2 Other means of identification

Product number -
Other names cis-4-trimethylsilanyl-cyclohexanol

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:7450-05-7 SDS

7450-05-7Relevant academic research and scientific papers

Trans-Selective and Switchable Arene Hydrogenation of Phenol Derivatives

Bergander, Klaus,Glorius, Frank,Heusler, Arne,Wollenburg, Marco

, p. 11365 - 11370 (2020/11/24)

A trans-selective arene hydrogenation of abundant phenol derivatives catalyzed by a commercially available heterogeneous palladium catalyst is reported. The described method tolerates a variety of functional groups and provides access to a broad scope of trans-configurated cyclohexanols as potential building blocks for life sciences and beyond in a one-step procedure. The transformation is strategically important because arene hydrogenation preferentially delivers the opposite cis-isomers. The diastereoselectivity of the phenol hydrogenation can be switched to the cis-isomers by employing rhodium-based catalysts. Moreover, a protocol for the chemoselective hydrogenation of phenols to cyclohexanones was developed.

S1P MODULATING AGENTS

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, (2014/08/19)

Compounds of formula (I) can modulate the activity of one or more S 1P receptors. Sphingosine 1-phosphate (S IP) is a lysophospholipid mediator that evokes a variety of cellular responses by stimulation of five members of the endothelial cell differentiation gene (EDG) receptor family, namely S1P1, S1P2, S1P3, S1P4, and S1P5 (formerly EDG1, EDG5, EDG3, EDG6 and EDG8). The EDG receptors are G-protein coupled receptors (GPCRs) and on stimulation propagate second messenger signals via activation of heterotrimeric G-protein alpha (Ga.) subunits and beta-gamma (G()y) dimers.

COMPOUNDS THAT ARE S1P MODULATING AGENTS AND/OR ATX MODULATING AGENTS

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, (2014/02/16)

Compounds of formula (I) can modulate the activity of one or more S1P receptors and/or the activity of autotaxin (ATX).

S1P MODULATING AGENTS

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Page/Page column 133-134, (2012/08/28)

Compounds of formula (I) or (II) can modulate the activity of SIP receptors.

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