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Benzene, 1-(2-butoxyethenyl)-4-chloro-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111615-87-3

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111615-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111615-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,6,1 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 111615-87:
(8*1)+(7*1)+(6*1)+(5*6)+(4*1)+(3*5)+(2*8)+(1*7)=93
93 % 10 = 3
So 111615-87-3 is a valid CAS Registry Number.

111615-87-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-butoxy-(E)-1-ethenyl)-4-chlorobenzene

1.2 Other means of identification

Product number -
Other names 1-((E)-2-Butoxy-vinyl)-4-chloro-benzene

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:111615-87-3 SDS

111615-87-3Relevant academic research and scientific papers

Poly(ethylene glycol) (PEG) as a Reusable Solvent Medium for Organic Synthesis. Application in the Heck Reaction

Chandrasekhar,Narsihmulu,Shameem Sultana,Ramakrishna Reddy

, p. 4399 - 4401 (2007/10/03)

(Matrix Presented) PEG has been used as a solvent medium for regioselective Heck reactions with easy recyclability of solvent and Pd catalyst for the first time.

Synthesis of β-Arylvinyl Ethers by the Palladium-Catalyzed Reaction of Aroyl Chlorides with Vinyl Ethers

Andersson, Carl-Magnus,Hallberg, Anders

, p. 235 - 239 (2007/10/02)

Reaction of aroyl chlorides with butyl vinyl ether in the presence of a palladium catalyst and an amine base affords β-arylvinyl ethers in 40-60percent yield.Both with regard to regioselectivity and reaction rate, aroyl chlorides were superior to aryl bro

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