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243670-10-2

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243670-10-2 Usage

Chemical Class

Polycyclic Aromatic Hydrocarbon (PAH) compound

Structure

Complex and highly aromatic with two hydroxyl groups at positions 2 and 10

Fused Ring Compound

Yes

Presence in

Coal tar and various types of combustion products

Environmental Pollutant

Yes, potent environmental pollutant

Carcinogenicity

Potential carcinogen

Handling and Disposal

Requires careful handling and disposal to prevent harm to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 243670-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,3,6,7 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 243670-10:
(8*2)+(7*4)+(6*3)+(5*6)+(4*7)+(3*0)+(2*1)+(1*0)=122
122 % 10 = 2
So 243670-10-2 is a valid CAS Registry Number.

243670-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,10-Dihydroxy-dibenzo[a,j]perylene-8,16-dione

1.2 Other means of identification

Product number -
Other names 2,10-dihydroxydibenzo[a,j]perylene-8,16-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:243670-10-2 SDS

243670-10-2Relevant articles and documents

Far-red dibenzo[a,j]perylene-8,16-dione dyes as fluorescent enzyme substrates and tags for biomolecules

Deady, Leslie W.,Hughes, Andrew B.,Mahadevan, Indumathy B.,Quazi, Nurul H.,Tilley, Leann M.

, p. 803 - 820 (2007/10/03)

The synthesis of fluorescent 2,10-derivatives of the title chromophore are described. The substituents contain amino-reactive N-hydroxysuccinimde ester and thiol-reactive iodoacetamide groups for attachment to biomolecules. A phosphate derivative was also prepared as an enzyme substrate.

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