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2045-79-6

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2045-79-6 Usage

Chemical Properties

clear yellow to slightly brown liquid

Uses

2-Methoxyphenethylamine can be used as HIV inhibitors and related viruses.

General Description

2-Methoxyphenethylamine (MPEA) is also referred to as o-methoxyphenethylamine. The distribution behavior of tyramine and MPEA in the [bmim][PF6]/water system (bmim = 1-butyl-3-methylimidazolium hexafluorophosphate) has been evaluated under different conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 2045-79-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,4 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2045-79:
(6*2)+(5*0)+(4*4)+(3*5)+(2*7)+(1*9)=66
66 % 10 = 6
So 2045-79-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO/c1-11-9-5-3-2-4-8(9)6-7-10/h2-5H,6-7,10H2,1H3/p+1

2045-79-6 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (M0844)  2-(2-Methoxyphenyl)ethylamine  >98.0%(GC)(T)

  • 2045-79-6

  • 5mL

  • 330.00CNY

  • Detail
  • TCI America

  • (M0844)  2-(2-Methoxyphenyl)ethylamine  >98.0%(GC)(T)

  • 2045-79-6

  • 25mL

  • 880.00CNY

  • Detail

2045-79-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methoxyphenethylamine

1.2 Other means of identification

Product number -
Other names 2-Methoxy-benzeneethanamine

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:2045-79-6 SDS

2045-79-6Relevant articles and documents

Direct Primary Amination of Alkylmetals with NH-Oxaziridine

Behnke, Nicole Erin,Kielawa, Russell,Kwon, Doo-Hyun,Ess, Daniel H.,Kürti, László

supporting information, p. 8064 - 8068 (2019/01/04)

A method for the primary electrophilic amination of primary, secondary, and tertiary organometallic substrates from a bench-stable NH-oxaziridine reagent is described. This facile and highly chemoselective transformation occurs at ambient temperature and without transition metal catalysts or purification by column chromatography to provide alkylamine products in a single step. Density functional theory (DFT) calculations revealed that, despite the basicity of alkylmetals, the direct NH-transfer pathway is favored over proton and O-transfer.

17a-HYDROXYLASE/C17,20-LYASE INHIBITORS

-

Paragraph 0350, (2014/03/21)

The present invention provides compounds of Formula (I), or a pharmaceutically acceptable salt thereof, where R1, R2, R3, R4, R5, R6, A and n are as defined herein. A deuteriated derivative of the compound of Formula (I) is also provided.

Process for the preparation of (8As,12AS,13AS)-decahydroisoquino ((2,1-G) (1,6)-naphthyridin-8-one derivatives

-

, (2008/06/13)

The invention provides a process for preparing single enantiomers of compounds represented by the formula: STR1 and chiral acid addition salts thereof; wherein: X and Y are independently hydrogen; lower alkyl; lower alkoxy; or halo; or X and Y taken together is methylenedioxy or ethylene-1,2-dioxy; which includes reduction of a compound represented by the formula: STR2 to give a mixture of stereoisomers represented by the formula: STR3 wherein each wavy line independently represents a bond in either the α or β position; followed by dissolving the mixture of stereoisomers and a chiral resolving acid in a suitable solvent and allowing the solution to crystallize, giving a salt of the desired enantiomer.

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