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34982-21-3

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34982-21-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34982-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,9,8 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34982-21:
(7*3)+(6*4)+(5*9)+(4*8)+(3*2)+(2*2)+(1*1)=133
133 % 10 = 3
So 34982-21-3 is a valid CAS Registry Number.

34982-21-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3,3,3-triphenylpropanoate

1.2 Other means of identification

Product number -
Other names Triphenylmethylessigsaeuremethylester

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:34982-21-3 SDS

34982-21-3Relevant articles and documents

Hexameric resorcinarene capsule is a bronsted acid: Investigation and application to synthesis and catalysis

Zhang, Qi,Tiefenbacher, Konrad

, p. 16213 - 16219 (2013/11/19)

Molecular capsules have attracted interest as simple enzyme mimetics and several examples of catalytic transformations in water-soluble metal-ligand based systems have been reported. This is not the case for hydrogen-bond based molecular capsules, which in contrast can be employed in organic solvents. We describe herein our investigations of such a system: The resorcin[4]arene hexamer is one of the largest hydrogen bond-based self-assembled capsules and has been studied intensively due to its ready availability. We present evidence that the capsule acts as a reasonably strong Bronsted acid (pK a approximately 5.5-6). This finding explains the capsule's high affinity toward tertiary amines that are protonated and therefore encounter cation-π interactions inside the cavity. We were able to translate this finding into a first synthetic application: A highly substrate-selective Wittig reaction. We also report that this property renders the capsule an efficient enzyme-like catalyst for substrate selective diethyl acetal hydrolysis.

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