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N-(Cyclohexylmethyl)-N-methylcyclopropanamine is a complex organic compound with the molecular formula C12H23N. It is a derivative of cyclopropanamine, featuring a cyclohexylmethyl group attached to the nitrogen atom, and a methyl group on the adjacent carbon. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is an important intermediate in the production of certain drugs and can be used in the development of new chemical entities with specific therapeutic or pesticidal properties. The compound's structure and properties make it a valuable building block in the field of organic chemistry, particularly in the creation of molecules with specific biological activities.

7584-68-1

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7584-68-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7584-68-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,8 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7584-68:
(6*7)+(5*5)+(4*8)+(3*4)+(2*6)+(1*8)=131
131 % 10 = 1
So 7584-68-1 is a valid CAS Registry Number.

7584-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(cyclohexylmethyl)-N-methylcyclopropanamine

1.2 Other means of identification

Product number -
Other names N-Cyclopropyl-N-methylcyclohexanemethylamine

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:7584-68-1 SDS

7584-68-1Downstream Products

7584-68-1Relevant academic research and scientific papers

Cytochrome P450-catalyzed oxidation of N-benzyl-N-cyclopropylamine generates both cyclopropanone hydrate and 3-hydroxypropionaldehyde via hydrogen abstraction, not single electron transfer

Cerny, Matthew A.,Hanzlik, Robert P.

, p. 3346 - 3354 (2007/10/03)

The suicide substrate activity of N-benzyl-N-cyclopropylamine (1) and N-benzyl-N-(1′-methylcyclopropyl)amine (2) toward cytochrome P450 and other enzymes has been explained by a mechanism involving single electron transfer (SET) oxidation, followed by rin

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