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1-bromo-2-naphthyl diphenylmethyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

433684-74-3

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433684-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 433684-74-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,3,6,8 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 433684-74:
(8*4)+(7*3)+(6*3)+(5*6)+(4*8)+(3*4)+(2*7)+(1*4)=163
163 % 10 = 3
So 433684-74-3 is a valid CAS Registry Number.

433684-74-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-2-naphthyl diphenylmethyl ether

1.2 Other means of identification

Product number -
Other names -

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:433684-74-3 SDS

433684-74-3Relevant academic research and scientific papers

Control of tandem isomerizations: Flow-assisted reactions of: O -lithiated aryl benzyl ethers

Lee, Hyune-Jea,Kim, Heejin,Yoshida, Jun-Ichi,Kim, Dong-Pyo

supporting information, p. 547 - 550 (2018/01/19)

Tandem chemical changes are often difficult to control at will, because they proceed rapidly through multiple unstable reactive intermediates. It is desirable to develop a novel method for controlling such tandem changes to obtain desired products with high selectivity. Herein, we report a flow microreactor platform for controlling tandem isomerizations of o-lithiated aryl benzyl ethers based on precise residence time control.

On the Reactivity of o-Lithioaryl Ethers: Tandem Anion Translocation and Wittig Rearrangement

Barluenga, Jose,Fananas, Francisco J.,Sanz, Roberto,Marcos, Cesar,Trabada, Marta

, p. 1587 - 1590 (2007/10/03)

(matrix presented) Allyl and benzyl 2-lithioaryl ethers, generated by bromine-lithium exchange in THF, undergo a new tandem anion translocation-[1,2]-Wittig rearrangement allowing the isolation of the corresponding benzylic alcohols.

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