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90791-37-0

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90791-37-0 Usage

Class

Anthracene derivatives

Molecular Structure

Contains an amino group, a methoxy group, and a phenylamino group

Application

Fluorescent dye used in biochemical and cell biology studies

Uses

Detecting protein binding, DNA interactions, and membrane potential changes

Additional Use

Staining agent in histology and cytology

Hazardous Nature

Potentially hazardous

Handling Precaution

Should be handled with care due to potential toxicity and environmental impact

Check Digit Verification of cas no

The CAS Registry Mumber 90791-37-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,9 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90791-37:
(7*9)+(6*0)+(5*7)+(4*9)+(3*1)+(2*3)+(1*7)=150
150 % 10 = 0
So 90791-37-0 is a valid CAS Registry Number.

90791-37-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-amino-4-anilino-2-methoxyanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 1-amino-4-anilino-2-methoxy-anthracene-9,10-dione

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:90791-37-0 SDS

90791-37-0Downstream Products

90791-37-0Relevant articles and documents

PHYSICAL CHARACTERISTICS OF SYNTHESIZED 1-AMINO-4-(ARYLAMINO)ANTHRAQUINONE 2-ETHER DYES FOR SYNTHETIC-POLYMER FIBERS.

Ukponmwan,Greenhalgh,Peters

, p. 482 - 483 (2007/10/02)

The synthesis and characteristics of a series of 2-ethers of 1-amino-4-(arylamino)anthraquinone by various preparative routes are described. Replacement of a bromine atom in the beta -position by a phenoxy group increased the molecular size.

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