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13662-06-1

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13662-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13662-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,6 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13662-06:
(7*1)+(6*3)+(5*6)+(4*6)+(3*2)+(2*0)+(1*6)=91
91 % 10 = 1
So 13662-06-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H12O2/c1-10(14)9-15-13-7-6-11-4-2-3-5-12(11)8-13/h2-8H,9H2,1H3

13662-06-1SDS

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 1-naphthalen-2-yloxypropan-2-one

1.2 Other means of identification

Product number -
Other names [2]naphthyloxy-acetone

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:13662-06-1 SDS

13662-06-1Downstream Products

13662-06-1Relevant articles and documents

Discovery of oxime-bearing naphthalene derivatives as a novel structural type of Nrf2 activators

Chang, Ken-Ming,Liang, Fong-Pin,Chen, I-Li,Yang, Shyh-Chyun,Juang, Shin-Hun,Wang, Tai-Chi,Chen, Yeh-Long,Tzeng, Cherng-Chyi

, p. 3852 - 3859 (2015)

Abstract Recent studies have demonstrated that oxidative stress insult is one of major causes of tumor formation. Therefore, identify the effective anti-oxidative agents as a preventive approach to stop cancer progression has widely explored. Although, ma

Catalytic Wacker-type Oxidations Using Visible Light Photoredox Catalysis

Ho, Yee Ann,Paffenholz, Eva,Kim, Hyun Jin,Orgis, Benjamin,Rueping, Magnus,Fabry, David C.

, p. 1889 - 1892 (2019/03/17)

A combined palladium/photoredox catalytic system for the efficient oxidation of terminal olefins to the corresponding methyl ketones is presented. The interplay of air, water, and light leads to a protocol in which the stoichiometric oxidants required for oxidative palladium catalysis are substituted with catalytic, single-electron transfer processes. Detailed mechanistic investigations revealed the role of the key components, in situ generated species, and catalysts. A broad range of substrates was examined in homogeneous as well as heterogeneous photoredox protocols, delivering the desired products in good yields.

Synthesis of methyl ketones from terminal olefins using PdCl 2/CrO3 system mimicking the Wacker process

Fernandes, Rodney A.,Bethi, Venkati

, p. 4760 - 4767 (2014/06/24)

An efficient synthesis of methyl ketones from terminal olefins using PdCl2/CrO3 system mimicking the Wacker process is developed. The method shows good functional groups compatibility, no aldehyde by-products and is operationally simple. CrO3 is the sole oxidant and replaces both Cu-salts and molecular oxygen, traditionally used in this process. The method holds potential for future applications in organic synthesis.

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