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1H-Xanthene, dodecahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58237-02-8

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58237-02-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58237-02-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,3 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58237-02:
(7*5)+(6*8)+(5*2)+(4*3)+(3*7)+(2*0)+(1*2)=128
128 % 10 = 8
So 58237-02-8 is a valid CAS Registry Number.

58237-02-8SDS

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 2,3,4,4a,5,6,7,8,8a,9,9a,10a-dodecahydro-1H-xanthene

1.2 Other means of identification

Product number -
Other names 1H-Xanthene,dodecahydro

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:58237-02-8 SDS

58237-02-8Upstream product

58237-02-8Downstream Products

58237-02-8Relevant academic research and scientific papers

A stable and practical nickel catalyst for the hydrogenolysis of C-O bonds

Cui, Xinjiang,Yuan, Hangkong,Junge, Kathrin,Topf, Christoph,Beller, Matthias,Shi, Feng

, p. 305 - 310 (2017/01/24)

The selective hydrogenolysis of C-O bonds constitutes a key step for the valorization of biomass including lignin fragments. Moreover, this defunctionalization process offers the possibility of producing interesting organic building blocks in a straightforward manner from oxygenated compounds. Herein, we demonstrate the reductive hydrogenolysis of a wide variety of ethers including diaryl, aryl-alkyl and aryl-benzyl derivatives catalyzed by a stable heterogeneous NiAlOx catalyst in the presence of a Lewis acid (LA). The special feature of this catalyst system is the formation of substituted cyclohexanols from the corresponding aryl ether.

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