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3077-14-3

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3077-14-3 Usage

General Description

1-[(4-methylphenyl)amino]-2-Propanol, also known as N-methylamphetamine, is a chemical compound with the molecular formula C10H15NO. It is a derivative of amphetamine and belongs to the class of substituted amphetamines. 1-[(4-methylphenyl)amino]-2-Propanol is commonly used as a pharmaceutical intermediate in the synthesis of various drugs, including sympathomimetic amines and psychostimulants. It has also been identified as a metabolite of methamphetamine and amphetamine in urine samples. Its chemical structure consists of a propanol group attached to a phenyl ring with a methyl group substitution and an amino group. The compound may have potential implications in the field of medicine and forensic toxicology due to its pharmacological activity and presence as a metabolite in drug screenings.

Check Digit Verification of cas no

The CAS Registry Mumber 3077-14-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,7 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3077-14:
(6*3)+(5*0)+(4*7)+(3*7)+(2*1)+(1*4)=73
73 % 10 = 3
So 3077-14-3 is a valid CAS Registry Number.

3077-14-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methylanilino)propan-2-ol

1.2 Other means of identification

Product number -
Other names 1-p-tolylamino-2-propanol

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:3077-14-3 SDS

3077-14-3Relevant articles and documents

The synthesis and substituent effect of the acid catalyzed hydrolysis of amidosulfites

Kutuk, Halil,Bekdemir, Yunus,Turkoz, Nalan

, p. 931 - 937 (2006)

The acid-catalyzed hydrolysis of 2-oxo-3-(p-substituted)-phenyl-5-methyl-1, 2,3-oxathiazolidines (1) have been studied in 60% (v/v) 1,4 dioxane-aqueous solutions of perchloric and hydrochloric acids at 10.0 ± 0.05°C. The analysis of the kinetic data by th

Post-synthesis of Zr-MOR as a robust solid acid catalyst for the ring-opening aminolysis of epoxides

Tang, Bo,Song, Wei-Chao,Li, Sheng-Yang,Yang, En-Cui,Zhao, Xiao-Jun

, p. 13503 - 13511 (2018/08/21)

Zirconosilicate with the MOR topology (Zr-MOR) was successfully prepared using a two-step post-synthesis strategy from pre-dealumination of a H-MOR zeolite and subsequent dry impregnation of Cp2ZrCl2. The incorporated Zr species main

Efficient solvent-free aminolysis of epoxides under (C4H 12N2)2[BiCl6]Cl·H 2O catalysis

Lu, Hong-Fei,Sun, Lei-Lei,Le, Wen-Jun,Yang, Fei-Fei,Zhou, Jun-Tao,Gao, Yu-Hua

experimental part, p. 4267 - 4272 (2012/09/22)

An efficient and rapid procedure for ring opening of various epoxides with aromatic, aliphatic and heterocyclic amines is developed at room temperature under solvent-free conditions in the presence of (C4H 12N2)2[BiCl6]Cl·H 2O (1 mol %). This catalyst can be reused several times without losing of its activity.

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