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Ethyl (2-phenoxyethylthio)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108655-75-0

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108655-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108655-75-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,6,5 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 108655-75:
(8*1)+(7*0)+(6*8)+(5*6)+(4*5)+(3*5)+(2*7)+(1*5)=140
140 % 10 = 0
So 108655-75-0 is a valid CAS Registry Number.

108655-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl (2-phenoxyethylthio)acetate

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:108655-75-0 SDS

108655-75-0Relevant academic research and scientific papers

Novel syntheses of 2,3-dihydro-5H-1,4-benzoxathiepins using polymer-supported bis(trifluoroacetoxyiodo)benzene

Huang, Hsin-Yu,Wang, Huey-Min,Hou, Rei-Sheu,Chen, Ling-Ching

, p. 1025 - 1028 (2004)

Pummerer-type reaction was carried out with α-acylsulfides and polymer-supported bis(trifluoroacetoxyiodo)benzene (PSBTI) instead of α-acylsulfoxides to prepare 2,3-dihydro-5H-1,4-benzoxathiepins.

Elimination and Addition Reactions. 36. Acceleration of Nucleophilic Eliminative Ring Fission by Bond Strain

Palmer, Robert J.,Stirling, Charles J. M.

, p. 7888 - 7892 (2007/10/02)

Rates of eliminative ring fission of cyclic ethers bearing carbanion stabilizing groups have been measured with a view to assessing the contribution of ring strain to the ease of cleavage of bonds in elimination reactions. (Ethylsulfonylmethyl)oxiran (4)

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