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342889-50-3

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342889-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 342889-50-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,8,8 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 342889-50:
(8*3)+(7*4)+(6*2)+(5*8)+(4*8)+(3*9)+(2*5)+(1*0)=173
173 % 10 = 3
So 342889-50-3 is a valid CAS Registry Number.

342889-50-3SDS

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 4,4'-bis(4-hydroxy-1-methyl-4-piperidinyl)biphenyl

1.2 Other means of identification

Product number -
Other names -

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:342889-50-3 SDS

342889-50-3Downstream Products

342889-50-3Relevant articles and documents

Syntheses and photophysical properties of some 4-arylpyridinium salts

Kelley,Ansu,Budisusetyo,Ghiorghis,Qin,Kauffman

, p. 11 - 23 (2007/10/03)

A number of 4-arylpyridines, many methoxy substituted, were prepared by an efficient two-step method involving aryl Grignard addition to 1-methyl-4-piperidone and direct aromatization of the resulting 4-aryl-4-piperidinols. The pyridines were N-alkylated to give sulfonate salts desired for their fluorescent properties. Study of selected compounds as laser dyes revealed several structures to be efficient dyes lasing in the 530-550 nm range. Two new diazaquaterphenyls were prepared and were quaternized. These salts exhibited intense fluorescence in the 420-450 nm range, but would not lase. A phenolic azaterphenyl suitably substituted for excited state intramolecular proton transfer (ESIPT) did not fluoresce at all.

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