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58520-45-9

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58520-45-9 Usage

Chemical Properties

white to off-white crystals, crystalline

Uses

(1R,2S)-1,2-Bis(4-methoxyphenyl)ethane-1,2-diamine is a fluorogenic reagent for reducing carbohydrates

Check Digit Verification of cas no

The CAS Registry Mumber 58520-45-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,2 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58520-45:
(7*5)+(6*8)+(5*5)+(4*2)+(3*0)+(2*4)+(1*5)=129
129 % 10 = 9
So 58520-45-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H20N2O2/c1-19-13-7-3-11(4-8-13)15(17)16(18)12-5-9-14(20-2)10-6-12/h3-10,15-16H,17-18H2,1-2H3/p+2/t15-,16+

58520-45-9 Well-known Company Product Price

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  • Sigma-Aldrich

  • (15025)  meso-1,2-Bis(4-methoxyphenyl)ethylenediamine  for HPLC derivatization, ≥98.0% (NT)

  • 58520-45-9

  • 15025-1G

  • 11,272.95CNY

  • Detail

58520-45-9SDS

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 (1R,2S)/(1S,2R)-1,2-diamino-1,2-bis(4-methoxyphenyl)ethane

1.2 Other means of identification

Product number -
Other names 1,2-ETHANEDIAMINE,1,2-BIS(4-METHOXYPHENYL)-, (1R,2S)-REL-

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:58520-45-9 SDS

58520-45-9Relevant articles and documents

Reductive coupling of aromatic oxims and azines to 1,2-diamines using Zn-MsOH or Zn-TiCl4

Kise, Naoki,Ueda, Nasuo

, p. 2365 - 2368 (2007/10/03)

The reduction of aromatic aldoxims and azines with Zn in the presence of MsOH or TiCl4 afforded N,N′-unsubstituted 1,2-diamines in one-step. The reductive coupling with Zn-MsOH gave meso 1,2-diamines selectively, whereas dl 1,2-diamines were fo

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