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62456-34-2

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62456-34-2 Usage

General Description

8-Bromonaphthalen-1-ylamine is a chemical compound with the molecular formula C10H8BrN. This organic compound is a derivative of naphthalene, with a bromine atom substituted at the 8-position and an amine functional group attached to the 1-position. It is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. 8-Bromonaphthalen-1-ylamine is also used in the production of dyes, pigments, and other organic compounds. It is important to handle this chemical with care, as it can be hazardous if it comes into contact with the skin, eyes, or respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 62456-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,5 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62456-34:
(7*6)+(6*2)+(5*4)+(4*5)+(3*6)+(2*3)+(1*4)=122
122 % 10 = 2
So 62456-34-2 is a valid CAS Registry Number.

62456-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-bromonaphthalen-1-amine

1.2 Other means of identification

Product number -
Other names 1-amino-8-bromonaphthalene

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:62456-34-2 SDS

62456-34-2Relevant articles and documents

FORMATION OF PERI-FUSED HETEROCYCLES BY INTRAMOLECULAR DISPLACEMENT OF HALIDE

Herbert, John M.,Woodgate, Paul D.,Denny, William A.

, p. 1037 - 1041 (2007/10/02)

The preparation of phthaloperin-12-one and naphtho-1,3-thiazine using copper-assisted displacement of aryl halogen is described.

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