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50822-99-6

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50822-99-6 Usage

Structure

2-(4-methoxyphenyl)-N,N,N-trimethylethanaminium chloride consists of a methoxyphenyl group attached to an N,N,N-trimethylethanaminium cation and a chloride anion.

Type of compound

Quaternary ammonium salt

Charge

The nitrogen atom in the compound has a positive charge, and it is balanced by the negatively charged chloride anion.

Uses

It is commonly used as a phase transfer catalyst in organic synthesis, aiding in the transfer of reactants between immiscible phases, and has potential applications in drug delivery systems and as an antimicrobial agent.

Physical properties

It is a colorless to pale yellow crystalline solid that is soluble in water and organic solvents.

Check Digit Verification of cas no

The CAS Registry Mumber 50822-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,2 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50822-99:
(7*5)+(6*0)+(5*8)+(4*2)+(3*2)+(2*9)+(1*9)=116
116 % 10 = 6
So 50822-99-6 is a valid CAS Registry Number.

50822-99-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxyphenyl)ethyl-trimethylazanium,chloride

1.2 Other means of identification

Product number -
Other names 4-Methoxy-N,N,N-trimethylbenzeneethanaminium chloride

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:50822-99-6 SDS

50822-99-6Downstream Products

50822-99-6Relevant articles and documents

Compound 48/80. Structure activity relations and poly THIQ, a new, more potent analog

Read,Kiefer,Weber

, p. 1292 - 1295 (2007/10/04)

Derivatives of p methoxyphenethylmethylamine were synthesized from which formaldehyde copolymers analogous to compound 48/80 were prepared. Measurement of the hypotensive activity of these analogs revealed that potency was not enhanced by changing the group in the para position, by varying the length of the alkyl group, or by altering the degree of methylation of the amine. However, when the ethylamine side chain was cyclized to form 7 methoxytetrahydroisoquinoline, the copolymer prepared from this derivative (poly THIQ) was seven times more potent than compound 48/80. The hypotensive action of poly THIQ was found to result from the liberation of histamine, as with compound 48/80.

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