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62889-09-2

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62889-09-2 Usage

Type of Compound

Symmetric biaryl ether and furan derivative

Physical State

Colorless liquid

Odor

Faint characteristic odor

Solubility

Insoluble in water, soluble in organic solvents

Uses

Intermediate in the synthesis of pharmaceuticals, production of liquid crystals and dyes

Toxicity

Toxic, may cause skin and eye irritation upon contact

Environmental Hazard

Potential environmental hazard due to toxicity to aquatic life.

Check Digit Verification of cas no

The CAS Registry Mumber 62889-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,8 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62889-09:
(7*6)+(6*2)+(5*8)+(4*8)+(3*9)+(2*0)+(1*9)=162
162 % 10 = 2
So 62889-09-2 is a valid CAS Registry Number.

62889-09-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-bis(furan-2-yl)furan

1.2 Other means of identification

Product number -
Other names Terfuranne-2,5

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:62889-09-2 SDS

62889-09-2Relevant articles and documents

Uebergangsmetallaktivierte organische Verbindungen, IX. Synthese von Polyfuranen durch metallorganische oxidative Kupplung

Kauffmann, Thomas,Lexy, Herbert,Kriegesmann, Reinhard

, p. 3667 - 3673 (2007/10/02)

2,2'- (2a) and 3,3'-bifuran (3), hitherto only accessible by ring-forming syntheses in small yields, and the unknown compounds all-α-terfuran (2b) and all-α-quaterfuran (2c) have been prepared by convenient ring-connecting syntheses in 85, 46, 16, or 53percent-yield, respectively.Lithiation of 2a and subsequent reacting with iodine afforded 5-iodo-2,2'-bifuran (6b, 46percent).According to competition experiments acidity against n-butyllithium is increasing in the sequence furan 2a 2b.

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