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125363-55-5

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125363-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125363-55-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,3,6 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 125363-55:
(8*1)+(7*2)+(6*5)+(5*3)+(4*6)+(3*3)+(2*5)+(1*5)=115
115 % 10 = 5
So 125363-55-5 is a valid CAS Registry Number.

125363-55-5SDS

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 2-(1-Fluoroethyl)-3-methyl oxirane

1.2 Other means of identification

Product number -
Other names 2-(1-Fluoro-ethyl)-3-methyl-oxirane

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:125363-55-5 SDS

125363-55-5Downstream Products

125363-55-5Relevant articles and documents

Complexes of cyclic polyaza chelators with cations of alkaline earth metals for enhanced biological activity

-

Page/Page column 10, (2010/02/11)

Cyclic polyaza chelators that possess high affinity and specificity for first transition series metal cations exhibit an unanticipated improvement in biological activity when administered as complexes with cations of the alkaline earth metals, Ca(II) and Mg(II), most notably Ca(II). By virtue of this improvement, these complexes are particularly effective in the treatment of pathological conditions, including ischemia and ischemia-reperfusion injury.

BROMOFLUORATION DES ALCOOLS ALLYLIQUES PAR NBS/Et3N, 3HF : UNE VOIE SIMPLE D'ACCES AUX EPIFLUORHYDRINES

Chehidi, Ikram,Chaabouni, Mohamed Moncef,Baklouti, Ahmed

, p. 3167 - 3170 (2007/10/02)

Bromofluorination of allylic alcohols using a combination of N-bromosuccinimide and triethlyamine tris-hydrofluoride gives the vicinal fluorobromohydrins.The treatment of the formed fluorobromohydrins with aqueous sodium hydroxide constitutes a convenient route to epifluorohydrins.

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