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N-(2-methyl-1-phenylpropan-2-yl)butan-1-amine is a complex organic compound with the molecular formula C15H23N. It is a derivative of butan-1-amine, where the nitrogen atom is bonded to a 2-methyl-1-phenylpropan-2-yl group. N-(2-methyl-1-phenylpropan-2-yl)butan-1-amine is characterized by its amine functional group and a branched alkyl chain with a phenyl ring attached. It is a colorless liquid at room temperature and is soluble in organic solvents. Due to its amine group, it can participate in various chemical reactions, such as acid-base reactions and nucleophilic substitutions. The compound may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals, although its specific uses would depend on further research and development.

5531-46-4

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5531-46-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5531-46-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,3 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5531-46:
(6*5)+(5*5)+(4*3)+(3*1)+(2*4)+(1*6)=84
84 % 10 = 4
So 5531-46-4 is a valid CAS Registry Number.

5531-46-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-butyl-2-methyl-1-phenylpropan-2-amine

1.2 Other means of identification

Product number -
Other names D-3-8

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:5531-46-4 SDS

5531-46-4Downstream Products

5531-46-4Relevant academic research and scientific papers

Inhibition of synaptosomal accumulation of l norepinephrine II: N aryloxyalkylphentermines, quaternary d amphetamines, and 3 aryloxypropylamines

Schaeffer,Cho,Fischer

, p. 122 - 126 (2007/10/06)

The inhibitory potencies of a series of N substituted phentermines on the synaptosomal uptake of l norepinephrine were found to be similar to those of the corresponding amphetamines. Quaternization of N,N dimethyl d amphetamine diminished, but did not abolish, its inhibitory potency, indicating that a permanently charged cation is also effective. Since the addition of an aromatic moiety at the end of a four atom chain originating at the nitrogen of amphetamine or phentermine significantly increased inhibitor strength, several 3 aryloxypropylamines and 4 phenylbutylamine were tested, but they were much weaker inhibitors than dl amphetamine. Thus, the observed increase in inhibitor potency apparently was not simply the result of a specific interaction of the 'nonmimic' portion of the N substituted amphetamines or phentermines.

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