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118670-83-0

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118670-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118670-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,7 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 118670-83:
(8*1)+(7*1)+(6*8)+(5*6)+(4*7)+(3*0)+(2*8)+(1*3)=140
140 % 10 = 0
So 118670-83-0 is a valid CAS Registry Number.

118670-83-0SDS

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 N-(2-iodophenyl)-N-(prop-2-enyl)acetamide

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:118670-83-0 SDS

118670-83-0Relevant articles and documents

1,3-disubstituted indoline derivative and preparation method thereof

-

Paragraph 0079; 0080; 0081, (2020/02/27)

The invention relates to a 1,3-disubstituted indoline derivative and a preparation method thereof, and belongs to the field of organic compound synthesis. The preparation method comprises following steps: step one, according to a mole ratio of (1-3): (2-1

Enantioselective Intramolecular C?H Insertion of Donor and Donor/Donor Carbenes by a Nondiazo Approach

Zhu, Dong,Ma, Jun,Luo, Kui,Fu, Hongguang,Zhang, Li,Zhu, Shifa

supporting information, p. 8452 - 8456 (2016/07/19)

The first enantioselective intramolecular C?H insertion and cyclopropanation reactions of donor- and donor/donor-carbenes by a nondiazo approach are reported. The reactions were conducted in a one-pot manner without slow addition and provided the desired

Indole and quinoline synthesis via intramolecular Pauson-Khand reactions of enamines and allylamines

Dominguez, Gema,Casarrubios, Luis,Rodriguez-Noriega, Javier,Perez-Castells, Javier

, p. 2856 - 2861 (2007/10/03)

Syntheses of indoles and quinolines based upon the Pauson-Khand reaction is described. The starting materials are an aromatic ethynylenamine and ethynylallylamine, which are obtained via Sonogashira coupling. Also, an aromatic ynamine is used for an attem

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