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63915-82-2

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63915-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63915-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,9,1 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63915-82:
(7*6)+(6*3)+(5*9)+(4*1)+(3*5)+(2*8)+(1*2)=142
142 % 10 = 2
So 63915-82-2 is a valid CAS Registry Number.

63915-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-1-[[4-[(1-methylpiperidin-1-ium-1-yl)methyl]phenyl]methyl]piperidin-1-ium,dibromide

1.2 Other means of identification

Product number -
Other names -

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:63915-82-2 SDS

63915-82-2Downstream Products

63915-82-2Relevant articles and documents

Structural investigation of bromide complexation with bipodal, tripodal and tetrapodal cationic molecules

Ling, Irene,Loh, Sze Le,Moggach, Stephen A.,Sobolev, Alexandre N.,Turner, Gemma F.

, p. 5539 - 5549 (2020)

Nine multipodal cationic molecules with adaptable cyclic and acyclic amine functional groups along with bromide as the counterion have been synthesised and structurally characterised by single crystal X-ray diffraction. In the solid-state, the dicationic bipodal molecule has a pincer-like geometry while the tricationic tripodal molecule has a cavity-like geometry. The tetracationic tetrapodal molecule crystallised as the chair conformer as a result of steric crowding by the heterocyclic amine functional groups (imidazolium and pyrrolidinium), which prohibits arrangement of the heterocyclic amine substituents in the same direction. This study also illustrates that the different packing motifs (including linear and corrugated layers, and channels) are affected by the substituents at the central core for each type of multipodal molecule. CrystalExplorer was used to visualise these weak intermolecular interactions and to quantitatively summarise the interactions that contribute to the overall stability to the crystal structure. This journal is

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