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16414-63-4

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16414-63-4 Usage

General Description

1-aminopropan-2-one 4-methylbenzenesulfonate (1:1) is a chemical compound that consists of a one-to-one ratio of the organic compound 1-aminopropan-2-one and 4-methylbenzenesulfonic acid. 1-aminopropan-2-one, also known as 2-Acetamidopropane, is a colorless liquid with a faint amine odor, and it is used as a reagent in organic synthesis. The 4-methylbenzenesulfonate component is a derivative of toluene sulfonic acid, a strong organic acid that is commonly used as a catalyst or as a reagent in various chemical reactions. When these two compounds are combined in a 1:1 ratio, they form an ionic compound with potential applications in organic synthesis or as a reagent in chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 16414-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,1 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16414-63:
(7*1)+(6*6)+(5*4)+(4*1)+(3*4)+(2*6)+(1*3)=94
94 % 10 = 4
So 16414-63-4 is a valid CAS Registry Number.

16414-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-aminopropan-2-one,4-methylbenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names 1-aminopropan-2-one para-toluenesulfonate

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:16414-63-4 SDS

16414-63-4Downstream Products

16414-63-4Relevant articles and documents

An optimized version of Gabriel-type nucleophilic amination

Zwierzak, Andrzej

, p. 2287 - 2293 (2007/10/03)

N-Alkylation of primary alkyl bromides with diethyl N-sodio-N-(t- butoxycarbonyl)phosphoramidate 1 carried out in boiling acetonitrile in the presence of 10mol% of tetrabutylammonium bromide as catalyst leads to the corresponding N-alkyl derivatives 2a-I. Deprotection of 2 by refluxing with p-toluenesulfonic acid in ethanol-affords ammonium tosylates 3a-I in reasonable yields.

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