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33458-36-5

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33458-36-5 Usage

Uses

Ethanethiol-SD (CAS# 33458-36-5) is a useful isotopically labeled research compound.

Check Digit Verification of cas no

The CAS Registry Mumber 33458-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,5 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 33458-36:
(7*3)+(6*3)+(5*4)+(4*5)+(3*8)+(2*3)+(1*6)=115
115 % 10 = 5
So 33458-36-5 is a valid CAS Registry Number.

33458-36-5SDS

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 ETHANETHIOL-SD

1.2 Other means of identification

Product number -
Other names N-desmethyl-escitalopram

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:33458-36-5 SDS

33458-36-5Relevant articles and documents

Thermoneutral Isotope Exchange Reactions of Cations in the Gas Phase

Ausloos, P.,Lias, S. G.

, p. 3641 - 3647 (2007/10/02)

Rate constants have been measured for reactions of the type AD2+ + MH --> MD + ADH+, where AD2+ is CD3CND+, CD3CDOD+, (CD3COCD3)D+, or (C2D5)2OD+ and the MH molecules are alcohols, acids, mercaptanes, H2S, AsH3, PH3, or aromatic molecules.Rate constants are also presented for the reactions ArHD+ + D2O --> ArDD+ + HDO, where ArHD+ is a deuteronated aromatic molecule and ArDD+ is the same species with a D atom incorporated on the ring.In all but two cases, the competing deuteron transfer is sufficiently endothermic that it cannot be observed under the conditions of the ICR experiments at 320 - 420 K.The efficiencies of the isotope exchange reactions are interpreted in terms of estimated potential surface cross sections for the reactions AD2+ + MH --> 2+*MH> --> +> --> +*MD> --> ADH+ + MD.When the formation of the +> complex is estimated to be thermoneutral or slightly endothermic, the isotope exchange process is inefficient (probability of a reactive collision 2+*MH> --> +> is exothermic.For most of the systems, trends in reaction efficiency appear to be related to factors such as dipole moments of reactant species (or for aromatic compounds, the electron-donating or -withdrawing properties of ring substituents) which influence the relative orientation of the two reactant species in the complex.

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