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388622-50-2

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388622-50-2 Usage

Derivative of

Naphthalenediol

Used in

Production of dyes and pharmaceuticals

Addition of

Fluorine atom

Known for

Unique properties

Properties

Increased chemical and thermal stability, altered reactivity

Potential uses

Materials science, pharmaceutical research

Further studies needed

To fully understand its properties and potential applications

Check Digit Verification of cas no

The CAS Registry Mumber 388622-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,8,6,2 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 388622-50:
(8*3)+(7*8)+(6*8)+(5*6)+(4*2)+(3*2)+(2*5)+(1*0)=182
182 % 10 = 2
So 388622-50-2 is a valid CAS Registry Number.

388622-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-fluoro-1,6-dihydroxynaphthalene

1.2 Other means of identification

Product number -
Other names 5-Fluoro-naphthalene-1,6-diol

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:388622-50-2 SDS

388622-50-2Downstream Products

388622-50-2Relevant articles and documents

Synthesis and photophysical properties of new fluorinated benzo[c]xanthene dyes as intracellular pH indicators

Liu, Jixiang,Diwu, Zhenjun,Leung, Wai-Yee

, p. 2903 - 2905 (2007/10/03)

Two new fluorinated benzo[c]xanthene dyes were synthesized by reaction of fluorinated 1,6-dihydroxynaphthalenes with 2,4- (and 2,5)-dicarboxy-3′-dimethylamino-2′-hydroxybenzophenone. The two critical fluorinated 1,6-dihydroxynaphthalene intermediates were prepared via a regioselective route. The fluorinated benzo[c]xanthene dyes exhibit desired lower pKa values (6.4 and 7.2, respectively) than their parent compound (pKa = 7.5) while the pH-dependent dual-emission characteristics are well retained. Their cell-permeable esters have been prepared for intracellular applications.

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