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86456-16-8

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86456-16-8 Usage

Family

Xanthene dyes

Appearance

Fluorescent dye

Usage

a. Tracer in water and air flow studies
b. Fluorescence microscopy
c. Biological stain
d. Textile industry (dye for silk, wool, and nylon)
e. Food industry (color additive for cosmetics, drugs, and lipsticks)

Additional Applications

a. Chemical intermediate in optical brighteners
b. Chemical intermediate in pesticides
c. Chemical intermediate in pharmaceuticals

Health Concerns

Potential carcinogenicity and adverse effects on humans and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 86456-16-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,5 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86456-16:
(7*8)+(6*6)+(5*4)+(4*5)+(3*6)+(2*1)+(1*6)=158
158 % 10 = 8
So 86456-16-8 is a valid CAS Registry Number.

86456-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-(dimethylamino)ethylamino]-7-methoxyxanthen-9-one

1.2 Other means of identification

Product number -
Other names 1-(2-dimethylaminoethylamino)-7-methoxyxanthen-9-one

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:86456-16-8 SDS

86456-16-8Relevant articles and documents

Analogues of hycanthone and lucanthone as antitumor agents

Archer,Zayed,Rej,Rugino

, p. 1240 - 1246 (2007/10/02)

Hycanthone analogues (5 and 6) containing 7-substituted hydroxyl groups were prepared and evaluated as antitumor agents. These compounds were significantly more active than the corresponding unsubtituted derivatives. The 7-hydroxylated-4-(hydroxymethyl)-9H-xanthen-9-ones, 11 and 12, were also active antitumor agents. However, the 7-hydroxy-9H-xanthen-9-one counterparts of the 7-hydroxylucanthones were totally devoid of antitumor activity. Results obtained thus far are consistent with the hypothesis that 4-hydroxymethyl substituents in the 9H-xanthen-9-one and 9H-thioxanthen-9-one series are required for antitumor activity.

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