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90799-47-6

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90799-47-6 Usage

Properties

1. Chemical compound
2. Naphthalene derivative
3. Contains amino group at 2-position
4. Contains chlorine atom at 7-position
5. Intermediate in synthesis of organic compounds
6. Used in manufacturing high-performance pigments
7. Utilized in development of functional materials
8. Reagent in chemical reactions

Specific content

Belongs to class of naphthalene derivatives
Used as intermediate in synthesis of organic compounds
Commonly used in manufacturing dyes, pharmaceuticals, and agrochemicals
Plays a role in production of fluorescent yellow dyes
Building block in development of functional materials
Reagent in chemical reactions for formation of complex molecules

Check Digit Verification of cas no

The CAS Registry Mumber 90799-47-6 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 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90799-47:
(7*9)+(6*0)+(5*7)+(4*9)+(3*9)+(2*4)+(1*7)=176
176 % 10 = 6
So 90799-47-6 is a valid CAS Registry Number.

90799-47-6SDS

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 7-chloronaphthalen-2-amine

1.2 Other means of identification

Product number -
Other names 2-Amino-7-chloronaphthalene

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:90799-47-6 SDS

90799-47-6Downstream Products

90799-47-6Relevant articles and documents

Synthesis of Aryl Amine Derivatives from Benzyl Nitriles via Electrocyclization of in Situ Generated N-Silyl Ketene Imines

Yoshimura, Fumihiko,Abe, Taiki,Tanino, Keiji

supporting information, p. 1630 - 1633 (2016/04/26)

The previously unexplored reactivity of N-silyl ketene imines in organic synthesis is reported. Benzyl nitriles containing an alkenyl or aryl group at the ortho position were smoothly converted into aryl amines in good yields under two sets of mild silyla

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