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66178-40-3

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66178-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66178-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,7 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66178-40:
(7*6)+(6*6)+(5*1)+(4*7)+(3*8)+(2*4)+(1*0)=143
143 % 10 = 3
So 66178-40-3 is a valid CAS Registry Number.

66178-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name deuterio methanesulfonate

1.2 Other means of identification

Product number -
Other names Methane sulfonic acid-d

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:66178-40-3 SDS

66178-40-3Downstream Products

66178-40-3Relevant articles and documents

Direct Spectroscopic Detection of Sulfonyloxy Radicals and First Measurements of Their Absolute Reactivities

Korth, Hans-Gert,Neville, Anthony G.,Lusztyk, Janusz

, p. 8835 - 8839 (2007/10/02)

Two sulfonyloxyl radicals, CH3S(=O)2O., 2a, and 3-CF3C6H4S(=O)2O., 2b, have been generated by 308-nm laser flash photolysis (LFP) of their parent symmetrical peroxides in CH3CN solution, in which they have lifetimes of 7-20 μs.Both radicals exhibit a broad, structureless absorption similar to that known for SO4.- with λmax ca. 450 nm.This absorption can be bleached for 2a but not for 2b by firing a second laser at 480 nm, presumably reflecting a photoinduced cleavage of the H3C-SO3. bond.Radicals 2a and 2b react with the acetonitrile solvent by abstraction of a hydrogen atom, kH ca. 1.6*105 M-1 s-1, kH/kD ca. 2.0.Bimolecular rate constants for attack of these radicals on cyclohexane (viz., 1.9*108 and 6.5*108 M-1 s-1 for 2a and 2b, respectively) and chloroform (viz. ca., 3*105 M-1 s-1 for both) demonstrate that they are more reactive than almost all other oxygen-centered radicals.Product studies demonstrate that both the photodecomposition and the thermal decomposition of the parent peroxides yield the corresponding sulfonyloxy radicals, a result that contrasts with that we have previously obtained for the decomposition of 2, which yields radicals on photolysis but few if any radicals on thermolysis.Semiempirical AM1/PM3-UHF calculations on 2a are also reported.

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