Welcome to LookChem.com Sign In|Join Free
  • or
2-{[(E)-(4-methoxyphenyl)methylidene]amino}-3-phenylpropan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17817-56-0

Post Buying Request

17817-56-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

17817-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17817-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,1 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17817-56:
(7*1)+(6*7)+(5*8)+(4*1)+(3*7)+(2*5)+(1*6)=130
130 % 10 = 0
So 17817-56-0 is a valid CAS Registry Number.

17817-56-0SDS

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)methylideneamino]-3-phenylpropan-1-ol

1.2 Other means of identification

Product number -
Other names 1-Propanol,2-((p-methoxybenzylidene)amino)-3-phenyl

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:17817-56-0 SDS

17817-56-0Downstream Products

17817-56-0Relevant academic research and scientific papers

Substituent effects in ring-chain tautomerism of the condensation products of non-racemic 1,2-aminoalcohols with aromatic aldehydes

Juhasz, Marta,Lazar, Laszlo,Fueloep, Ferenc

experimental part, p. 2012 - 2017 (2012/03/22)

The condensation of (S)-2-amino-2-phenylethanol or (S)-2-amino-3- phenylpropanol with substituted benzaldehydes in methanol or water led to crystalline products, which proved to exist in CDCl3 at 300 K as three-component (ringcis-ope

A novel one-pot procedure for the stereoselective synthesis of α-hydroxy esters from ortho esters

Breunlng, Matthias,Haeuser, Tobte,Tanzer, Eva-Maria

supporting information; experimental part, p. 4032 - 4035 (2009/12/09)

A novel one-pot procedure for the stereoselective synthesis of a-hydroxy esters from ortho esters was developed. Key steps were multiheteroatom Cope rearrangements of O-acylated N-hydroxy-L-tert-leucinol-derived oxazoline N-oxides leading to a-acyloxy oxazolines and, after methanolysis, to the target molecules in 67-80% yield and 94-98% ee.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 17817-56-0