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594-52-5

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594-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 594-52-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 594-52:
(5*5)+(4*9)+(3*4)+(2*5)+(1*2)=85
85 % 10 = 5
So 594-52-5 is a valid CAS Registry Number.

594-52-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-2,3-dimethylbutane

1.2 Other means of identification

Product number -
Other names NILGDLGIGRGWRL-UHFFFAOYSA

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:594-52-5 SDS

594-52-5Relevant articles and documents

High quantum yield molecular bromine photoelimination from mononuclear platinum(IV) complexes

Raphael Karikachery, Alice,Lee, Han Baek,Masjedi, Mehdi,Ross, Andreas,Moody, Morgan A.,Cai, Xiaochen,Chui, Megan,Hoff, Carl D.,Sharp, Paul R.

, p. 4113 - 4119 (2013/05/09)

Pt(IV) complexes trans-Pt(PEt3)2(R)(Br)3 (R = Br, aryl and polycyclic aromatic fragments) photoeliminate molecular bromine with quantum yields as high as 82%. Photoelimination occurs both in the solid state and in solution. Calorimetry measurements and DFT calculations (PMe3 analogs) indicate endothermic and endergonic photoeliminations with free energies from 2 to 22 kcal/mol of Br2. Solution trapping experiments with high concentrations of 2,3-dimethyl-2-butene suggest a radical-like excited state precursor to bromine elimination.

Reactions of a Graded Set of Radicals with N-Bromosuccinimide; Two Transition States

Tlumak, Robert L.,Skell Philip S.

, p. 7267 - 7274 (2007/10/02)

The reactions of N-bromosuccinimide with a series of radicals have been studied.These reactions fall into two categories, the more reactive radicals producing ?-succinimidyl and the less reactive radicals producing ?-succinimidyl.The threshold for the changeover from one reaction domain to the other occurs with radicals less reactive than secondary alkyls.These results are interpreted with two transition states, an in-line transition state for the more reactive radicals and an out-of-plane transition state for the less reactive radicals. An upper limit of 18 kcal/mol is established for the enthalpy difference, HS? - HS?.Two new methods for generating S? radicals are indicated.

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