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80355-66-4

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80355-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80355-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,5 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 80355-66:
(7*8)+(6*0)+(5*3)+(4*5)+(3*5)+(2*6)+(1*6)=124
124 % 10 = 4
So 80355-66-4 is a valid CAS Registry Number.

80355-66-4SDS

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 4-methyl-2-(1,2,3,4-tetrahydronaphthalen-1-yl)phenol

1.2 Other means of identification

Product number -
Other names Phenol,4-methyl-2-(1,2,3,4-tetrahydro-1-naphthalenyl)

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:80355-66-4 SDS

80355-66-4Downstream Products

80355-66-4Relevant articles and documents

Secondary benzylation with benzyl alcohols catalyzed by a high-valent heterobimetallic Ir-Sn complex

Podder, Susmita,Choudhury, Joyanta,Roy, Sujit

, p. 3129 - 3132 (2008/02/07)

(Chemical Equation Presented) A highly efficient secondary benzylation procedure has been demonstrated using a high-valent heterobimetallic complex [Ir2(COD)2(SnCls)2(Cl)2(μ-Cl) 2] 1 as the catalyst in 1,2-dichloroethane to afford the corresponding benzylated products in moderate to excellent yields. The reaction was performed not only with carbon nucleophiles (arenes and heteroarenes) but also with oxygen (alcohol), nitrogen (amide and sulfonamide), and sulfur (thiol) nucleophiles. Mechanistic investigation showed the intermediacy of the ether in this reaction. An electrophilic mechanism is proposed from Hammett correlation.

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