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13557-11-4

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13557-11-4 Usage

Physical state

Colorless liquid

Uses

Synthetic intermediate in production of pharmaceuticals, agrochemicals, and other fine chemicals; solvent in organic synthesis; fragrance ingredient in perfumes and personal care products

Toxicity

Low acute toxicity

Hazards

Potential hazards should be considered when handling and working with the compound

Compatibility

Versatile and compatible with a variety of chemical reactions

Applications

Wide range of applications in various industries, including the production of fragrances and organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 13557-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,5 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13557-11:
(7*1)+(6*3)+(5*5)+(4*5)+(3*7)+(2*1)+(1*1)=94
94 % 10 = 4
So 13557-11-4 is a valid CAS Registry Number.

13557-11-4SDS

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 2-[2-(oxan-2-yloxy)phenoxy]oxane

1.2 Other means of identification

Product number -
Other names 1,2-Bis-tetrahydropyran-2-yloxy-benzol

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:13557-11-4 SDS

13557-11-4Downstream Products

13557-11-4Relevant articles and documents

Chromogenic and fluorogenic crown ether compounds for the selective extraction and determination of Hg(II)

Vaidya, Bikas,Zak, Jerzy,Bastiaans, Glenn J.,Porter, Marc D.,Hallman, Johnny L.,Nabulsi, Nabeel A. R.,Utterback, Marty D.,Strzelbicka, Bozena,Bartsch, Richard A.

, p. 4101 - 4111 (1995)

Two novel crown ether compounds, N,N′-bis(2-hydroxy-5-nitrobenzyl)-4,13-diazadibenzo-18-crown-6 (CCE) and N,N′-bis(7-hydroxy-4-methylcoumarin-8-methylene)-4,13-diazadibenzo-18- crown-6 (FCE), have been synthesized as potential reagents for the selective e

Strategies for the synthesis of bi- and triarylic materials starting from commercially available phenols

Chopa, Alicia B.,Silbestri, Gustavo F.,Lockhart, María T.

, p. 3865 - 3877 (2007/10/03)

A series of arylstannanes have been synthesized, through an SRN1 mechanism, in good to excellent yields (74%-99%) by the photostimulated reaction of trimethyl stannyl ion with substrates supporting different nucleofugal groups. The arylstannanes thus obtained were suitable intermediates for Stille cross-coupling reactions leading to asymmetric bi- and triaryl compounds in acceptable global yields. An attractive feature of this route is that simple commercially available benzenediols, chloro- and methoxy phenols might be useful starting substrates, leading the latter to higher global yields of products in fewer steps. The strategies proposed open a broad synthetic tool.

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