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2243-64-3

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2243-64-3 Usage

Uses

a. Production of dyes and pigments
b. Manufacturing of azo dyes
c. Synthesis of pharmaceutical compounds

Physical state

Solid, crystalline substance

Solubility

Insoluble in water, soluble in organic solvents

Safety precautions

a. Harmful if ingested
b. Harmful if inhaled
c. Harmful if absorbed through the skin
d. Proper handling and storage required
e. Proper disposal to prevent environmental contamination

Check Digit Verification of cas no

The CAS Registry Mumber 2243-64-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,4 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2243-64:
(6*2)+(5*2)+(4*4)+(3*3)+(2*6)+(1*4)=63
63 % 10 = 3
So 2243-64-3 is a valid CAS Registry Number.

2243-64-3SDS

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 naphthalene-1,7-diamine

1.2 Other means of identification

Product number -
Other names naphthalene-1,7-diyldiamine

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:2243-64-3 SDS

2243-64-3Downstream Products

2243-64-3Relevant articles and documents

Nickel-Catalyzed Synthesis of Primary Aryl and Heteroaryl Amines via C-O Bond Cleavage

Yue, Huifeng,Guo, Lin,Liu, Xiangqian,Rueping, Magnus

supporting information, p. 1788 - 1791 (2017/04/11)

A nickel-catalyzed protocol for the conversion of aryl and heteroaryl alcohol derivatives to primary and secondary aromatic amines via C(sp2)-O bond cleavage is described. The new amination protocol can be applied to a range of substrates bearing diverse functional groups and uses readily available benzophenone imines as an effective nitrogen source.

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