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13252-73-8

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13252-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13252-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,5 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13252-73:
(7*1)+(6*3)+(5*2)+(4*5)+(3*2)+(2*7)+(1*3)=78
78 % 10 = 8
So 13252-73-8 is a valid CAS Registry Number.

13252-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-tert-butylphenyl)hydroxylamine

1.2 Other means of identification

Product number -
Other names 4-tert-Butylphenylhydroxylamin

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:13252-73-8 SDS

13252-73-8Upstream product

13252-73-8Relevant articles and documents

Integrating replication processes with mechanically interlocked molecular architectures

Vidonne, Annick,Philp, Douglas

, p. 8464 - 8475 (2008/12/22)

A kinetic model for the integration of self-replication with the formation of a mechanically interlocked molecular architecture, namely a rotaxane, is presented. The logical steps required to convert this model into molecular structures through consideration of the design criteria highlighted by the model are discussed and executed. Ultimately, despite careful design, the rotaxane synthesised did not replicate as expected. The reasons for this failure are traced by experiment and computation to the sub-optimal association constant for the pseudorotaxane complex required to form the replicating rotaxane. Additionally, a deleterious supramolecular steric effect, operating through the proximity of the macrocyclic component of the pseudorotaxane to the transition state for the stoppering reaction is identified computationally.

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