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13132-28-0

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13132-28-0 Usage

Chemical composition

Consists of an acenaphthylene molecule with a nitro group attached to the 1 position.

Physical form

Pale yellow solid.

Solubility

Insoluble in water, soluble in organic solvents.

Uses

Primarily used as an intermediate in the synthesis of various organic compounds, such as dyes and pigments.

Hazardous nature

Known to be phototoxic and mutagenic, with potential harmful effects on human health and the environment.

Handling and disposal

Proper methods are necessary when working with 1-nitroacenaphthylene due to its hazardous nature.

Check Digit Verification of cas no

The CAS Registry Mumber 13132-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,3 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13132-28:
(7*1)+(6*3)+(5*1)+(4*3)+(3*2)+(2*2)+(1*8)=60
60 % 10 = 0
So 13132-28-0 is a valid CAS Registry Number.

13132-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-nitroacenaphthylene

1.2 Other means of identification

Product number -
Other names Acenaphthylene,1-nitro

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:13132-28-0 SDS

13132-28-0Upstream product

13132-28-0Downstream Products

13132-28-0Relevant articles and documents

-

Cantrell,T.S.,Shechter,H.

, p. 114 - 118 (1968)

-

Extended porphyrinoid chromophores: heteroporphyrins fused to phenanthrene and acenaphthylene

Lash, Timothy D.,Rauen, Patrick J.

, (2021/10/12)

Fusion of aromatic subunits onto porphyrin chromophores produces variable results and in some cases only minor bathochromic shifts are observed. In order to extend these observations, a series of oxa-, thia- and selenaporphyrins with fused acenaphthylene

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