Welcome to LookChem.com Sign In|Join Free

CAS

  • or

63179-93-1

Post Buying Request

63179-93-1 Suppliers

Recommended suppliersmore

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

63179-93-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63179-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,7 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63179-93:
(7*6)+(6*3)+(5*1)+(4*7)+(3*9)+(2*9)+(1*3)=141
141 % 10 = 1
So 63179-93-1 is a valid CAS Registry Number.

63179-93-1SDS

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 meso-5-exo,6-exo-dibromobicyclo[2.2.1]heptane-2-endo,3-endo-dicarboxylic anhydride

1.2 Other means of identification

Product number -
Other names exo,exo-5,6-dibromonorbornane-endo,endo-2,3-dicarboxylic anhydride

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:63179-93-1 SDS

63179-93-1Relevant articles and documents

The role of neat substrates in phase-vanishing and tandem phase-vanishing reactions

Windmon, Nicole,Dragojlovic, Veljko

scheme or table, p. 6543 - 6546 (2009/04/06)

Phase-vanishing reactions are triphasic reactions, which involve a reagent, a liquid perfluoroalkane as a phase screen and a substrate. Aromatization, isomerization and halogenation of neat substrates under phase-vanishing conditions gave the expected products in good to excellent yields. In tandem single-phase-phase-vanishing reaction, two reactants, placed in the top phase, afforded the intermediate, which in a subsequent phase-vanishing reaction reacted with the reagent from the bottom phase to give the final product. The reaction worked well under solvent-free conditions on liquid substrates and intermediates. With solids, results were better if an additional solvent was employed.

PHASE TRANSITIONS IN BICYCLIC COMPOUNDS.

Weinstein,Leffler,Currie

, p. 95 - 109 (2007/10/02)

The thermal properties of bicyclic and cyclic compounds obtained by DSC show that substituents such as the anhydride, nitrile, and carbonyl groups retain the polymorphic phase properties of the parent ring systems while groups such as the imide, methylimide, and carboxylic acid exclude the appearance of a disordered solid phase. The phase properties of chloro and hydroxyl derivatives investigated and more varied and depend on the position of these groups on the ring. The variety of compounds studied shows that hysteresis is a common occurrence in all of these ring systems.

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 63179-93-1