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1,3,2-Dioxarsolane, 2-phenoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58669-64-0

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58669-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58669-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,6 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58669-64:
(7*5)+(6*8)+(5*6)+(4*6)+(3*9)+(2*6)+(1*4)=180
180 % 10 = 0
So 58669-64-0 is a valid CAS Registry Number.

58669-64-0SDS

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 2-phenoxy-1,3,2-dioxarsolane

1.2 Other means of identification

Product number -
Other names 2-Phenoxy-[1,3,2]dioxarsolan

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:58669-64-0 SDS

58669-64-0Downstream Products

58669-64-0Relevant academic research and scientific papers

1H and 13C NMR Studies on 1,3,2-Dioxarsolanes

Aksnes, D. W.,Lie, A.

, p. 417 - 425 (2007/10/02)

The 1H and 13C NMR spectra of a series of 1,3,2-dioxarsolanes have been obtained at 2.1 T and some at 9.4 T.The chemical shifts and spin-spin coupling constants have been obtained from complete spectral analyses of the 1H and proton coupled 13C spectra.The spectral data are interpreted on the basis of two rapidly interconverting half-chair conformers with pseudoaxial substituent at arsenic.Unique assignment of syn/anti or cis/trans geometries have been made from 1H or 13C NMR spectroscopy alone.The syn and trans isomers of the 4-methyl- and 4,5-dimethyl-1,3,2-dioxarsolenes, respectively, appear to be conformationally biased towards the forms with pseudoequatorial methyl groups.The general trends in the geminal and vicinal 1H-1H and 13C-1H coupling constants are interpreted in terms of stereospecific, electronegativity and lone pair effects of the oxygen heteroatoms and conformational factors.The NMR data on the 1,3,2-dioxarsolanes are discussed with reference to related 1,3-dioxa- and 1,3-dithia- five-membered rings with As, P, S, or C at the 2-position.

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