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4621-04-9

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  • 4-ISO-PROPYLCYCLOHEXANOL CAS NO.4621-04-9 CAS NO.4621-04-9 CAS NO.4621-04-9 CAS NO.4621-04-9

    Cas No: 4621-04-9

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4621-04-9 Usage

General Description

4-ISO-PROPYLCYCLOHEXANOL, also known as 4-Isopropylcyclohexanol, is a chemical compound with the molecular formula C10H20O. It is a colorless liquid with a faint, peppermint-like odor. This chemical is commonly used as a fragrance ingredient in various personal care and cosmetic products. It is also used as a solvent in the manufacturing of paints, coatings, and adhesives. Additionally, 4-ISO-PROPYLCYCLOHEXANOL has applications in the production of plastics and rubber. It is important to handle this chemical with caution as it may cause irritation to the skin, eyes, and respiratory system upon exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 4621-04-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,2 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4621-04:
(6*4)+(5*6)+(4*2)+(3*1)+(2*0)+(1*4)=69
69 % 10 = 9
So 4621-04-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O/c1-7(2)8-3-5-9(10)6-4-8/h7-10H,3-6H2,1-2H3/t8-,9+

4621-04-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Isopropylcyclohexanol

1.2 Other means of identification

Product number -
Other names 4-ISO-PROPYLCYCLOHEXANOL

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:4621-04-9 SDS

4621-04-9Relevant articles and documents

Green,Roy

, p. 6368 (1970)

Hydrogenolysis of lignin model compounds into aromatics with bimetallic Ru-Ni supported onto nitrogen-doped activated carbon catalyst

Hu, Yinghui,Jiang, Guangce,Xu, Guoqiang,Mu, Xindong

, p. 316 - 326 (2018/01/05)

Lignin is the most abundant and renewable resources for production of natural aromatics. In this paper, new bimetallic catalytic system of Ru and Ni supported onto nitrogen-doped activated carbon (Ru-Ni-AC/N) was developed and its performances on hydrogenolysis of lignin model compounds under mild reaction conditions (1.0 MPa, 230 °C, in aqueous) were investigated. The results indicate that Ru-Ni-AC/N was a highly active, selective and stable catalyst for the conversion of lignin model compounds into aromatics, e.g. phenol, benzene and their derivatives. As verified by BET, XRD, HRTEM, XPS, H2-TPR and ICP-MS, the strong synergistic effects between i) Ru and Ni and ii) metals and N-groups were contributed to its excellent aromatics selectivity. What's more, the introduction of electron rich N atoms on AC was beneficial to the stabilization of metal particles, which greatly enhanced the durability of the catalyst.

Cytochrome P450 catalyzed oxidative hydroxylation of achiral organic compounds with simultaneous creation of two chirality centers in a single C-H activation step

Roiban, Gheorghe-Doru,Agudo, Ruben,Reetz, Manfred T.

supporting information, p. 8659 - 8663 (2014/08/18)

Regio- and stereoselective oxidative hydroxylation of achiral or chiral organic compounds mediated by synthetic reagents, catalysts, or enzymes generally leads to the formation of one new chiral center that appears in the respective enantiomeric or diastereomeric alcohols. By contrast, when subjecting appropriate achiral compounds to this type of C-H activation, the simultaneous creation of two chiral centers with a defined relative and absolute configuration may result, provided that control of the regio-, diastereo-, and enantioselectivity is ensured. The present study demonstrates that such control is possible by using wild type or mutant forms of the monooxygenase cytochrome P450 BM3 as catalysts in the oxidative hydroxylation of methylcyclohexane and seven other monosubstituted cyclohexane derivatives.

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