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Propane-1,1,1,3,3,3-d6, 2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74440-45-2

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74440-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74440-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,4 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74440-45:
(7*7)+(6*4)+(5*4)+(4*4)+(3*0)+(2*4)+(1*5)=122
122 % 10 = 2
So 74440-45-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H10/c1-4(2)3/h4H,1-3H3/i1D3,2D3

74440-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,3,3,3-hexadeuterio-2-methylpropane

1.2 Other means of identification

Product number -
Other names Propane-1,1,1,3,3,3-d6,2-methyl

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:74440-45-2 SDS

74440-45-2Downstream Products

74440-45-2Relevant academic research and scientific papers

Secondary Hydrogen Isotope Effect in the Unimolecular Decomposition of 2-Methylpropane Radical Cations

Mead, Phillip T.,Donchi, Kevin F.,Traeger, John C.,Christie, John R.,Derrick, Peter J.

, p. 3364 - 3369 (1980)

The intensities of the mass spectral metastable peaks for loss of methane from 2-methylpropane-1,1,1,3,3,3-d6 reveal a strong secondary hydrogen isotope effect, in that the rate of loss of CH3D is approximately an order of magnitude greater than the rate of loss of CD3H, which in turn is several times greater than the rate of loss of CD4.This isotope effect is interpreted in terms of a nonclassical transition state involving a three-center bond.This nonclassical structure is analogous to the transition state containing a three-center two-electron bond, belived to be involved in the reaction of 2-methylpropane with superacids.Photoionization appearance energies, determined for the molecular and fragment ions from 2-methylpropane, 2-methylpropane-2-d1, and 2-methylpropane-1,1,1,3,3,3-d6, and detailed rate calculations provide support for the nonclassical structure.

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