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6310-65-2

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6310-65-2 Usage

Class

Naphthalene derivatives

Use

Fluorescent tracer for visualizing and tracking molecules in biological systems

Structure

Naphthalene core with two dimethylamino groups attached to a benzyl group

Property

Emits strong fluorescent signal when excited by specific wavelengths of light

Applications

Cellular imaging, drug discovery, molecular biology research

Potential

Versatile and efficient tool for studying physiological processes and interactions within living organisms

Check Digit Verification of cas no

The CAS Registry Mumber 6310-65-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6310-65:
(6*6)+(5*3)+(4*1)+(3*0)+(2*6)+(1*5)=72
72 % 10 = 2
So 6310-65-2 is a valid CAS Registry Number.

6310-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[bis[4-(dimethylamino)phenyl]methyl]naphthalen-2-ol

1.2 Other means of identification

Product number -
Other names 1-{bis[4-(dimethylamino)phenyl]methyl}naphthalen-2-ol

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:6310-65-2 SDS

6310-65-2Downstream Products

6310-65-2Relevant articles and documents

SnBr4-promoted Friedel-Crafts type dehydrative alkylation reaction of diarylmethanols with 2-naphthol derivatives

Suzuki, Nobuharu,Tsuchihashi, Shiori,Nakata, Kenya

supporting information, p. 1456 - 1459 (2016/03/12)

Tin(IV) bromide was found to act as an efficient Lewis acid catalyst for the Friedel-Crafts type dehydrative alkylation reaction of diarylmethanols with 2-naphthol derivatives under mild conditions. The effects of the substituents on the substrates were systematically evaluated, and the reaction could be applied to a variety of substrates by tuning the conditions depending on the electronic properties of the starting materials.

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