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Propanoic acid, 2-chloro-3-(phenylseleno)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112701-63-0

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112701-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112701-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,0 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 112701-63:
(8*1)+(7*1)+(6*2)+(5*7)+(4*0)+(3*1)+(2*6)+(1*3)=80
80 % 10 = 0
So 112701-63-0 is a valid CAS Registry Number.

112701-63-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl α-chloro-β-(phenylseleno)propionate

1.2 Other means of identification

Product number -
Other names ethyl 2-chloro-3-phenylselanylpropanoate

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:112701-63-0 SDS

112701-63-0Downstream Products

112701-63-0Relevant academic research and scientific papers

Synthesis and reactivity of α and β-chloro-α-phenylselanyl esters

Lebarillier, Loic,Outurquin, Francis,Paulmier, Claude

, p. 7495 - 7502 (2000)

Thermal decomposition of the dichloro-adducts derived from α-phenylselanylesters 1, 2 and 4 has been studied. N-Chloro-succinimide treatment of esters 2 was an efficient preparative method for α-chloro-α-phenylselanylesters 10 and α-chloro-α,β-unsaturated esters 11. Some transformations of esters 10 were achieved, α,β-Dichloro-α-phenylselanylesters 22 were prepared from β-chloro-α-phenylselanylesters 5 or by decomposition of the dichloroselenuranes 21 derived from esters 4. (C) 2000 Elsevier Science Ltd.

Electrophilic Addition of Benzeneselenenyl Chloride to Alkenes Bearing an Electron-withdrawing Substituent

Toshimitsu, Akio,Terao, Keiji,Uemura, Sakae

, p. 1059 - 1062 (2007/10/02)

Reaction of benzeneselenenyl chloride with alkenes bearing electron-withdrawing substituents was found to afford a mixture of regioisomeric adducts formed via the electrophilic addition of the phenylseleno group.The isomer distribution can be accounted for by postulating the interaction in the episelenonium ion intermediate of the phenylseleno group with the electron-withdrawing substituent.

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