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(3,5-DIMETHOXY-BENZYL)-(4-METHOXY-BENZYL)-AMINE is a benzylamine derivative featuring methoxy groups at positions 3, 5, and 4 on the benzene ring. This unique structure and properties make it a promising candidate for organic synthesis and drug development.
Used in Organic Synthesis:
(3,5-DIMETHOXY-BENZYL)-(4-METHOXY-BENZYL)-AMINE is used as a building block for the synthesis of various organic molecules. Its versatile chemical structure allows for the preparation of new compounds with potential applications in different industries.
Used in Drug Development:
(3,5-DIMETHOXY-BENZYL)-(4-METHOXY-BENZYL)-AMINE is used as a starting material for the development of pharmaceutical drugs. Its unique structure may contribute to the creation of new compounds with potential biological activities and therapeutic benefits.
Used in Chemical Synthesis as a Reagent:
(3,5-DIMETHOXY-BENZYL)-(4-METHOXY-BENZYL)-AMINE is used as a reagent in chemical synthesis processes. Its properties make it a valuable component in the preparation of various chemical compounds.
Used in Medicinal Chemistry:
(3,5-DIMETHOXY-BENZYL)-(4-METHOXY-BENZYL)-AMINE is used in medicinal chemistry for the development of new pharmaceutical agents. Its potential as a versatile building block can lead to the discovery of innovative treatments and therapies.

356093-54-4

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356093-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 356093-54-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,6,0,9 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 356093-54:
(8*3)+(7*5)+(6*6)+(5*0)+(4*9)+(3*3)+(2*5)+(1*4)=154
154 % 10 = 4
So 356093-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H21NO3/c1-19-15-6-4-13(5-7-15)11-18-12-14-8-16(20-2)10-17(9-14)21-3/h4-10,18H,11-12H2,1-3H3

356093-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(3,5-dimethoxyphenyl)methyl]-1-(4-methoxyphenyl)methanamine

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:356093-54-4 SDS

356093-54-4Upstream product

356093-54-4Relevant academic research and scientific papers

Synthesis of the ABH rings of ecteinascidin 597 using a connective Pummerer-type cyclisation

Smith, Laura H. S.,Nguyen, Trung Thanh,Sneddon, Helen F.,Procter, David J.

, p. 10821 - 10823 (2011/11/05)

A connective Pummerer-type cyclisation involving a cysteine derivative and an N-benzyl glyoxamide 3 has been applied in an asymmetric synthesis of the protected ABH rings 2 of the antitumour and antimicrobial natural product ecteinascidin 597.

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