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604799-97-5

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604799-97-5 Usage

Chemical structure

A cyclopropane ring attached to a naphthalene ring and an amine group.

Molecular weight

219.31 g/mol

Fields of application

Pharmaceutical, agrochemical, and material sciences.

Role

Valuable building block in the synthesis of complex organic compounds.

Potential applications

Development of new drugs or as a precursor in the production of specialized chemicals.

Safety

Handle with care due to potential hazards and follow proper safety protocols when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 604799-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,4,7,9 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 604799-97:
(8*6)+(7*0)+(6*4)+(5*7)+(4*9)+(3*9)+(2*9)+(1*7)=195
195 % 10 = 5
So 604799-97-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H13N/c14-13(7-8-13)12-6-5-10-3-1-2-4-11(10)9-12/h1-6,9H,7-8,14H2

604799-97-5SDS

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 1-naphthalen-2-ylcyclopropan-1-amine

1.2 Other means of identification

Product number -
Other names -

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:604799-97-5 SDS

604799-97-5Downstream Products

604799-97-5Relevant articles and documents

A direct synthesis of 1-aryl- and 1-alkenylcyclopropylamines from aryl and alkenyl nitriles

Bertus, Philippe,Szymoniak, Jan

, p. 7133 - 7136 (2007/10/03)

The reaction of various aromatic nitriles with 1.1 equiv of Ti(Oi-Pr)4 and 2.2 equiv of EtMgBr followed by addition of a Lewis acid gave 1-aryl cyclopropylamines in 43-76% yields. Under similar conditions, conjugated alkene-nitriles afford 1-alkenylcyclopropylamines (42-65%).

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