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Phenol, 2-(ethenyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58981-47-8

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58981-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58981-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,8 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58981-47:
(7*5)+(6*8)+(5*9)+(4*8)+(3*1)+(2*4)+(1*7)=178
178 % 10 = 8
So 58981-47-8 is a valid CAS Registry Number.

58981-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethenoxyphenol

1.2 Other means of identification

Product number -
Other names 2-(vinyloxy)phenol

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:58981-47-8 SDS

58981-47-8Relevant academic research and scientific papers

Reductive opening of carbohydrate phenylsulfonylethylidene (PSE) acetals

Chéry, Florence,Cabianca, Elena,Tatibou?t, Arnaud,De Lucchi, Ottorino,Lindhorst, Thisbe K.,Rollin, Patrick

, p. 117 - 124 (2015/10/28)

The phenylsulfonylethylidene (PSE) acetal is a relatively new protecting group in carbohydrate chemistry. However, carbohydrate-derived phenylsulfonylethylidene (PSE) acetals show a different behavior in reductive desulfonylation than simple symmetrical a

A general, selective synthesis of ω-hydroxyethenyl ethers

Cabianca,Chéry,Rollin,Tatibou?t,De Lucchi

, p. 585 - 587 (2007/10/03)

A general selective synthesis of β-, γ- and δ-hydroxyethenyl ethers, a class of compounds containing two mutually reactive functionalities positioned at an interacting distance, is based on the reaction of diols with 1,2-bis-(phenylsulfonyl)ethylene (BPSE) followed by reductive elimination of the resulting β-phenylsulfonyl acetals with sodium amalgam.

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