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20009-27-2

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20009-27-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20009-27-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,0 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20009-27:
(7*2)+(6*0)+(5*0)+(4*0)+(3*9)+(2*2)+(1*7)=52
52 % 10 = 2
So 20009-27-2 is a valid CAS Registry Number.

20009-27-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-i-propoxylnaphthalene

1.2 Other means of identification

Product number -
Other names isopropyl-[1]naphthyl ether

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:20009-27-2 SDS

20009-27-2Relevant articles and documents

Exploiting ancillary ligation to enable nickel-catalyzed c-o cross-couplings of aryl electrophiles with aliphatic alcohols

MacQueen, Preston M.,Tassone, Joseph P.,Diaz, Carlos,Stradiotto, Mark

supporting information, p. 5023 - 5027 (2018/04/24)

The use of (L)Ni(o-tolyl)Cl precatalysts (L = PAd-DalPhos or CyPAd-DalPhos) enables the C(sp2)-O cross-coupling of primary, secondary, or tertiary aliphatic alcohols with (hetero)aryl electrophiles, including unprecedented examples of such nickel-catalyzed transformations employing (hetero)aryl chlorides, sulfonates, and pivalates. In addition to offering a competitive alternative to palladium catalysis, this work establishes the feasibility of utilizing ancillary ligation as a complementary means of promoting challenging nickel-catalyzed C(sp2)-O cross-couplings, without recourse to precious-metal photoredox catalytic methods.

One-pot synthesis of 4-alkoxybenzo[c]thiophenes

Akbarzadeh, Tahmineh,Shafiee, Abbas

, p. 1455 - 1462 (2007/10/03)

The reaction of N-bromosuccinimide with 4,5,6,7-tetrahydrobenzo[c]thiophen-4-ones in the presence of 2,2′-azo-bis-isobutyronitrile followed by heating under reflux with different alcohols produces 4-alkoxybenzo[c]thiophenes in good yield.

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