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106477-02-5

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106477-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106477-02-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,4,7 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106477-02:
(8*1)+(7*0)+(6*6)+(5*4)+(4*7)+(3*7)+(2*0)+(1*2)=115
115 % 10 = 5
So 106477-02-5 is a valid CAS Registry Number.

106477-02-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-tetralinyl tert-butylperoxide

1.2 Other means of identification

Product number -
Other names .1,2,3,4-tetrahydro-1-naphthyl tert-butyl peroxide

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:106477-02-5 SDS

106477-02-5Downstream Products

106477-02-5Relevant articles and documents

Copper catalyzed oxidation of tetralin to 1-(tert-butylperoxy)-tetralin by aqueous tert-butylhydroperoxide under phase transfer conditions

Feldberg, Liron,Sasson, Yoel

, p. 2063 - 2066 (1996)

Selective α-peroxidation of tetralin by TBHP is catalyzed by copper salts with the aid of quaternary ammonium compounds in an aqueous-organic biphasic system.

Rh2(esp)2-catalyzed allylic and benzylic oxidations

Wang, Yuanhua,Wang, Yi,Kuang, Yi

supporting information, p. 5852 - 5855 (2015/03/30)

The dirhodium(ii) catalyst Rh2(esp)2 allows direct solvent-free allylic and benzylic oxidations by T-HYDRO with a remarkably low catalyst loading. This method is operationally simple and scalable at ambient temperature without the use of any additives. The high catalyst stability in these reactions may be attributed to a dirhodium(ii,ii) catalyst resting state, which is less prone to decomposition.

Synthesis, single crystal structures and efficient catalysis for tetralin oxidation of two novel complexes of Cu(II) with 2-aminomethyl pyridine

Wang, Chunling,Zhang, Yuecheng,Yuan, Baoguo,Zhao, Jiquan

scheme or table, p. 173 - 179 (2011/02/24)

Two novel Cu(II) complexes were synthesized through the reaction of 2-aminomethyl pyridine (AMP) with CuCl2·2H2O by changing the metal/ligand ratio. Their structures were thoroughly characterized by FT-IR, elemental analysis and X-ray diffraction method. The results revealed that complex 1 [Cu(AMP)Cl2] consists of isolated binuclear molecules unit and displays distorted tetragonal pyramid. Complex 2 [Cu(AMP) 2(H2O)2]Cl2 exhibits a octahedral geometry. The complexes were both evaluated as catalysts in the tetralin oxidation with TBHP as oxidant. Complex 1 showed high catalytic activity and selectivity towards α-tetralone under mild conditions. Thus, under the optimized conditions (acetonitrile 10 ml, catalyst 0.045 mmol, tetralin 4.5 mmol, 65% TBHP 22.5 mmol, T = 50 °C), the conversion of tetralin reached 89% with a selectivity of 71% towards α-tetralone. Compared with complex 1, complex 2 displayed low catalytic activity mainly due to the strong steric hindrance from the two coordinated 2-aminomethyl pyridine molecules.

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