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O-3-iodophenyl N,N-diethylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

863870-73-9

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863870-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 863870-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,8,7 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 863870-73:
(8*8)+(7*6)+(6*3)+(5*8)+(4*7)+(3*0)+(2*7)+(1*3)=209
209 % 10 = 9
So 863870-73-9 is a valid CAS Registry Number.

863870-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name O-3-iodophenyl N,N-diethylcarbamate

1.2 Other means of identification

Product number -
Other names 3-iodophenyl diethylcarbamate

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:863870-73-9 SDS

863870-73-9Relevant academic research and scientific papers

Polyaromatic ribbons from oligo-alkynes via selective radical cascade: Stitching aromatic rings with polyacetylene bridges

Byers, Philip M.,Alabugin, Igor V.

, p. 9609 - 9614 (2012)

Selective radical generation in conjugated oligomeric o-aryleneethynylenes initiates an intramolecular cascade which involves five fast radical cyclizations followed by aromatization via a 1,5-H shift with a >93% yield per step. This radical cascade trans

How to Achieve High Regioselectivity in Barrier-less Nucleophilic Addition to p-Benzynes Generated via Bergman Cyclization of Unsymmetrical Cyclic Azaenediyne?

Das, Eshani,Basak, Shyam,Anoop, Anakuthil,Chand, Santanu,Basak, Amit

, p. 2911 - 2921 (2019/02/26)

Inducing high regioselectivity in nucleophilic addition to p-benzynes, first reported by Perrin and O'Connor et al. (J. Am. Chem. Soc. 2007, 129, 4795-4799) has been a challenge as the reaction involves a very fast barrier-less addition of nucleophile. On

Modular Synthesis of Graphene Nanoribbons And Graphene Substructures From Oligo-Alkynes

-

Paragraph 0101, (2013/05/09)

A method for the synthesis of carbon-based structures, particularly graphene substructures and ribbons, from oligo- and poly-alkyne starting materials.

A new and efficient synthesis of 4-functionalized benzo[6]furans from 2,3-dihalophenols

Sanz, Roberto,Castroviejo, M. Pilar,Fernandez, Yolanda,Fananas, Francisco J.

, p. 6548 - 6551 (2007/10/03)

Tandem Sonogashira coupling/5-endo-dig cyclization reactions on 2,3-dihalophenols suppose a straightforward entry to 4-halobenzo[b]furans, which can be easily transformed into 4-functionalized benzo[b]furans, that are difficult to synthesize by other proc

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