Welcome to LookChem.com Sign In|Join Free

CAS

  • or

71092-59-6

Post Buying Request

71092-59-6 Suppliers

Recommended suppliersmore

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

71092-59-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71092-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,9 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 71092-59:
(7*7)+(6*1)+(5*0)+(4*9)+(3*2)+(2*5)+(1*9)=116
116 % 10 = 6
So 71092-59-6 is a valid CAS Registry Number.

71092-59-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,7,10,13,16,19,22,25,28,31,34-dodecaoxacyclohexatriacontane

1.2 Other means of identification

Product number -
Other names 36-Crown-12

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:71092-59-6 SDS

71092-59-6Downstream Products

71092-59-6Relevant articles and documents

Synthesis and Characterization of Large (30-60-Membered) Aliphatic Crown Ethers

Gibson, Harry W.,Bheda, Mukesh C.,Engen, Paul,Shen, Ya Xi,Sze, Jean,et al.

, p. 2186 - 2196 (2007/10/02)

We report a new synthetic approach to large (30-72 membered) crown ethers based on isolation of the small and large cyclic polyethers made by combination of 1 mol or 2 mol each, respectively, of oligo(ethylene glycol)s and oligo(ethylene glycol) ditosylates.The advantages of this approach are the use of readily available glycols as starting materials and the ability to optimize the procedure for selective production of either macrocycle, producing yields superior or comparable to previous methods.At higher reaction temperatures the large crown ether is preferentially formed.This approach has been used to produce the crown ethers on 100-g scales.Purification was achieved by a combination of filtration through silica gel, treatment with a polymeric acid chloride, and recrystallization techniques, avoiding standard column chromatography.The pure crown ethers, 60-crown-20, 48-crown-16, 42-crown-14, 36-crown-12, and 30-crown-10, were characterized by melting points, 1H- and 13C-NMR, elemental analysis, and/or MS, GC-MS, and TGA-MS.Melting points were as much as 26 deg C higher than previously reported for these crown ethers.All the aliphatic crown ethers larger than 18-crown-6 decompose upon heating in air at ca. 200 deg C.

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 71092-59-6