Welcome to LookChem.com Sign In|Join Free

CAS

  • or

2635-26-9

Post Buying Request

2635-26-9 Suppliers

Recommended suppliersmore

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

2635-26-9 Usage

Chemical Properties

YELLOW FLAKES OR POWDER

Purification Methods

Purify azoxybenzene by chromatography on Al2O3 (*benzene), recrystallise it from hexane or 95% EtOH and dry it by heating under vacuum. The liquid crystals can be sublimed in vacuo. [Mellifiori et al. Spectrochim Acta Part A 37(A) 605 1981, Dewar & Schroeder J Am Chem Soc 86 5235 1964, Weygand & Glaber J Prakt Chem 155 332 1940, Beilstein 16 III 600, 16 IV 5264.]

Check Digit Verification of cas no

The CAS Registry Mumber 2635-26-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,3 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2635-26:
(6*2)+(5*6)+(4*3)+(3*5)+(2*2)+(1*6)=79
79 % 10 = 9
So 2635-26-9 is a valid CAS Registry Number.

2635-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-heptoxyphenyl)-(4-heptoxyphenyl)imino-oxidoazanium

1.2 Other means of identification

Product number -
Other names 4,4'-Bis(heptyloxy)azoxybenzene

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:2635-26-9 SDS

2635-26-9Downstream Products

2635-26-9Relevant articles and documents

The newborn surface of dull metals in organic synthesis. Bismuth-mediated solvent-free one-step conversion of nitroarenes to azoxy- and azoarenes

Wada, Shinobu,Urano, Mika,Suzuki, Hitomi

, p. 8254 - 8257 (2007/10/03)

When milled together with bismuth shots, nitroarenes are readily converted to azoxy- and/or azoarenes depending on substrates and conditions employed. Simple extraction with organic solvent followed by evaporation of the resulting dark pasty solid gave the product in good yield.

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

What can I do for you?
Get Best Price

Get Best Price for 2635-26-9