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2206-27-1 Usage

Chemical Properties

liquid

Uses

Different sources of media describe the Uses of 2206-27-1 differently. You can refer to the following data:
1. (Dimethyl Sulfoxide-d6) DMSO is a very common aprotic solvent that is used in a variety of organic chemical reactions and spectroscopic analyses.
2. DMSO-d6 is a solvent of choice in NMR spectroscopy, owing to its unique characteristics of dissolving both nonpolar and polar compounds, miscibility with almost all organic solvents and permitting high temperature dynamic NMR studies.
3. Dimethyl sulfoxide-d6 may be used as an NMR solvent for 1H and 13C NMR experiments.

General Description

Dimethyl sulfoxide-d6 (DMSO-d6) is a deuterated solvent. It is 100% isotopically enriched NMR (Nuclear Magnetic Resonance) solvent. It is widely employed in high resolution NMR studies due to its high chemical and isotopic purity. On photoirradiation in the range of 193 and 222nm, it undergoes decomposition to afford CD3 radicals. Quantum yields of CD3 have been evaluated by infrared diode laser absorption spectroscopy. 100% DMSO-d6 has been used as solvent in the long-range COSY (Correlation Spectroscopy) experiment.

Check Digit Verification of cas no

The CAS Registry Mumber 2206-27-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2206-27:
(6*2)+(5*2)+(4*0)+(3*6)+(2*2)+(1*7)=51
51 % 10 = 1
So 2206-27-1 is a valid CAS Registry Number.
InChI:InChI=1/C2H6OS/c1-4(2)3/h1-2H3/i1D3,2D3

2206-27-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (42285)  Dimethyl sulfoxide-d6, 100% (Isotopic)   

  • 2206-27-1

  • 2each

  • 480.0CNY

  • Detail
  • Alfa Aesar

  • (42285)  Dimethyl sulfoxide-d6, 100% (Isotopic)   

  • 2206-27-1

  • 10each

  • 1868.0CNY

  • Detail
  • Alfa Aesar

  • (42286)  Dimethyl sulfoxide-d6, 100% (Isotopic), contains 0.03% v/v TMS   

  • 2206-27-1

  • 2each

  • 492.0CNY

  • Detail
  • Alfa Aesar

  • (42286)  Dimethyl sulfoxide-d6, 100% (Isotopic), contains 0.03% v/v TMS   

  • 2206-27-1

  • 10each

  • 1991.0CNY

  • Detail
  • Alfa Aesar

  • (A16893)  Dimethyl sulfoxide-d6, 99.5% (Isotopic)   

  • 2206-27-1

  • 10g

  • 319.0CNY

  • Detail
  • Alfa Aesar

  • (A16893)  Dimethyl sulfoxide-d6, 99.5% (Isotopic)   

  • 2206-27-1

  • 50g

  • 1487.0CNY

  • Detail
  • Alfa Aesar

  • (36517)  Dimethyl sulfoxide-d6, 99.9% (Isotopic)   

  • 2206-27-1

  • *5x1g

  • 359.0CNY

  • Detail
  • Alfa Aesar

  • (36517)  Dimethyl sulfoxide-d6, 99.9% (Isotopic)   

  • 2206-27-1

  • *10x1g

  • 558.0CNY

  • Detail
  • Aldrich

  • (417939)  Dimethylsulfoxide-d6  "100%", 99.96 atom % D, contains 0.03 % (v/v) TMS

  • 2206-27-1

  • 417939-10X0.75ML

  • 2,059.20CNY

  • Detail
  • Aldrich

  • (417939)  Dimethylsulfoxide-d6  "100%", 99.96 atom % D, contains 0.03 % (v/v) TMS

  • 2206-27-1

  • 417939-25ML

  • 4,960.80CNY

  • Detail
  • Aldrich

  • (612324)  Dimethylsulfoxide-d6  "Special HOH", ≥99.9 atom % D

  • 2206-27-1

  • 612324-25G

  • 1,377.09CNY

  • Detail
  • Aldrich

  • (612324)  Dimethylsulfoxide-d6  "Special HOH", ≥99.9 atom % D

  • 2206-27-1

  • 612324-50G

  • 2,356.38CNY

  • Detail

2206-27-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethylsulfoxide-D6

1.2 Other means of identification

Product number -
Other names DMSO Dimethylsulfoxide-d6

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:2206-27-1 SDS

2206-27-1Synthetic route

1-[3-(t-butoxycarbonylaminomethyl)phenyl]-5-[(3-fluoro-2'-methylsulfonyl-[1,1']-biphen-4-yl)aminocarbonyl]-3-(methylthio)pyrazole

1-[3-(t-butoxycarbonylaminomethyl)phenyl]-5-[(3-fluoro-2'-methylsulfonyl-[1,1']-biphen-4-yl)aminocarbonyl]-3-(methylthio)pyrazole

A

dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

B

1-[3-(aminomethyl)phenyl]-5-[(3-fluoro-2'-methylsulfonyl-[1,1']-biphen-4-yl)aminocarbonyl]-3-(methylthio)pyrazole

1-[3-(aminomethyl)phenyl]-5-[(3-fluoro-2'-methylsulfonyl-[1,1']-biphen-4-yl)aminocarbonyl]-3-(methylthio)pyrazole

Conditions
ConditionsYield
With trifluoroacetic acid In dichloromethaneA n/a
B 92%
dimethyl sulfide-d6
926-09-0

dimethyl sulfide-d6

A

dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

B

((methyl-d3)sulfonyl)methane-d3
22230-82-6

((methyl-d3)sulfonyl)methane-d3

C

C2H(2)H5O2S

C2H(2)H5O2S

Conditions
ConditionsYield
With 5,10,15,20-tetrakisphenylporphyrin; oxygen In benzene for 1.33333h; Mechanism; Product distribution; Ambient temperature; Irradiation; var. irradiation times, var. solvent, also with addition H2O; other sulfides; kinetic isotope effect;A 5.2%
B n/a
C n/a
N,N'-dimethylbenzylamine
103-83-3

N,N'-dimethylbenzylamine

C2H(2)H6OS(1+)
103259-34-3

C2H(2)H6OS(1+)

A

dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

B

N,N-dimethylbenzylammonium ion
54061-38-0

N,N-dimethylbenzylammonium ion

Conditions
ConditionsYield
at 20℃; Equilibrium constant;
trifluoroacetate
14477-72-6

trifluoroacetate

C2H(2)H6OS(1+)
103259-34-3

C2H(2)H6OS(1+)

A

dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

B

trifluoroacetic acid
76-05-1

trifluoroacetic acid

Conditions
ConditionsYield
at 20℃; Equilibrium constant; Rate constant;
tris-trideuteriomethyl-sulfoxonium iodide

tris-trideuteriomethyl-sulfoxonium iodide

dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

Conditions
ConditionsYield
at 200℃; under 20 Torr;
C2H(2)H6OS
103259-34-3

C2H(2)H6OS

A

dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

B

((methyl-d3)sulfonyl)methane-d3
22230-82-6

((methyl-d3)sulfonyl)methane-d3

C

methyl-d3 peroxy radical

methyl-d3 peroxy radical

D

CH(2)H3OS

CH(2)H3OS

E

HO2, OH

HO2, OH

Conditions
ConditionsYield
With oxygen at -23.1℃; under 110 Torr; Rate constant; Irradiation;
With oxygen at -15.1℃; under 110 Torr; Rate constant; Irradiation;
[2,2]bipyridinyl
366-18-7

[2,2]bipyridinyl

1,3-cyclooctadiene
3806-59-5

1,3-cyclooctadiene

2-benzenesulfonyl-1,4-dibromobenzene
1312951-81-7

2-benzenesulfonyl-1,4-dibromobenzene

2,2'-bis-benzenesulfonyl-4,4'-dibromobiphenyl
1312951-82-8

2,2'-bis-benzenesulfonyl-4,4'-dibromobiphenyl

nickel(0)(1,5-cyclooctadiene)2

nickel(0)(1,5-cyclooctadiene)2

dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

Conditions
ConditionsYield
In methanol
cis-{PtCl2(d6-Me2SO)2}
154068-77-6

cis-{PtCl2(d6-Me2SO)2}

2-(2'-pyridyl)quinoxaline
7755-91-1

2-(2'-pyridyl)quinoxaline

A

dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

(2-(2'-pyridyl)quinoxaline)platinum(II) dichloride
194037-47-3

(2-(2'-pyridyl)quinoxaline)platinum(II) dichloride

Conditions
ConditionsYield
at 24.84℃; Equilibrium constant;
cis-{PtCl2(d6-Me2SO)2}
154068-77-6

cis-{PtCl2(d6-Me2SO)2}

2,(2'-pyridyl)benzo[g]quinoxaline

2,(2'-pyridyl)benzo[g]quinoxaline

A

dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

Pt(2,(2'-pyridyl)benzo[g]quinoxaline)Cl2

Pt(2,(2'-pyridyl)benzo[g]quinoxaline)Cl2

Conditions
ConditionsYield
at 24.84℃; Equilibrium constant;
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

[Ir{k2-N,C-(pyC(H)C(C(O)Me))}(CO)(μ-Cl)(Me)]2

[Ir{k2-N,C-(pyC(H)C(C(O)Me))}(CO)(μ-Cl)(Me)]2

[Ir{k2-N,C-(pyC(H)C(C(O)Me))}(CO)Cl(Me)DMSO]

[Ir{k2-N,C-(pyC(H)C(C(O)Me))}(CO)Cl(Me)DMSO]

Conditions
ConditionsYield
at 20℃; for 0.0833333h; Inert atmosphere; Schlenk technique;100%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

iodomethane-d3
865-50-9

iodomethane-d3

<2H9>trimethylsulphoxonium iodide
23726-00-3

<2H9>trimethylsulphoxonium iodide

Conditions
ConditionsYield
for 72h;98%
at 50℃; for 72h;29%
18%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

[2H8]bis(methylthio)methane

[2H8]bis(methylthio)methane

Conditions
ConditionsYield
Stage #1: dimethylsulfoxide-d6 With acetic anhydride at 130℃; for 1h; Sealed tube;
Stage #2: With sulfuric acid for 0.0833333h;
98%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

[MoO2Cl2(deuterated dimethyl sulfoxide)2]

[MoO2Cl2(deuterated dimethyl sulfoxide)2]

Conditions
ConditionsYield
In diethyl ether soln. of ligand in Et2O was added with stirring to soln. of Mo complex in Et2O; mixt. was stirred for 5 min; filtered; washed (Et2O); dried (vac.); elem. anal.;97%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

methacrylic acid-(4-iodo-anilide)
99071-31-5

methacrylic acid-(4-iodo-anilide)

C11H10(2)H3IN4O

C11H10(2)H3IN4O

Conditions
ConditionsYield
With ferrous(II) sulfate heptahydrate; trimethylsilylazide; dihydrogen peroxide at 50℃; for 3h; Inert atmosphere; Sealed tube;96%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

benzyl alcohol
100-51-6

benzyl alcohol

d-(E)-(2-(benzyloxy)vinyl)benzene
344740-75-6

d-(E)-(2-(benzyloxy)vinyl)benzene

Conditions
ConditionsYield
With potassium hydroxide at 20℃;95%
With potassium hydroxide; phenol at 60℃; for 12h; Green chemistry;65%
styrene
292638-84-7

styrene

dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

C9H7(2)H3O2S

C9H7(2)H3O2S

Conditions
ConditionsYield
With ammonium iodide; water at 130℃; for 24h; Sealed tube; Glovebox; stereoselective reaction;95%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

2-methyl-N-phenylacrylamide
1611-83-2

2-methyl-N-phenylacrylamide

C11H11(2)H3N4O

C11H11(2)H3N4O

Conditions
ConditionsYield
With ferrous(II) sulfate heptahydrate; trimethylsilylazide; dihydrogen peroxide at 50℃; for 3h; Inert atmosphere; Sealed tube;95%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

para-iodoanisole
696-62-8

para-iodoanisole

(4-methoxyphenyl)(methyl)sulfane-d3
24658-23-9

(4-methoxyphenyl)(methyl)sulfane-d3

Conditions
ConditionsYield
With copper(l) iodide; zinc diacetate at 135℃; for 24h; Reagent/catalyst; regioselective reaction;94%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

benzamide
55-21-0

benzamide

C15H12(2)H2N2O2

C15H12(2)H2N2O2

Conditions
ConditionsYield
With ammonium peroxydisulfate In 1,4-dioxane at 100℃; for 6h; Green chemistry;94%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

1-phenyl-2-tosylethanone
31378-03-7

1-phenyl-2-tosylethanone

C17H13(2)H5O3S2

C17H13(2)H5O3S2

Conditions
ConditionsYield
With acetic acid at 120℃; for 3h;93%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

2-[2-(2-bromophenyl)ethynyl]benzoate

2-[2-(2-bromophenyl)ethynyl]benzoate

3-(2-bromophenyl)-4-((methyl-d3)thio)-1H-isochromen-1-one

3-(2-bromophenyl)-4-((methyl-d3)thio)-1H-isochromen-1-one

Conditions
ConditionsYield
With thionyl chloride at 25℃; regioselective reaction;93%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

methyl 2-(phenylethynyl)benzoate
33578-05-1

methyl 2-(phenylethynyl)benzoate

4-((methyl-d3)thio)-3-phenyl-1H-isochromen-1-one

4-((methyl-d3)thio)-3-phenyl-1H-isochromen-1-one

Conditions
ConditionsYield
With thionyl chloride at 25℃;92%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

2-(2-phenylethynyl)benzoate

2-(2-phenylethynyl)benzoate

4-((methyl-d3)thio)-3-phenyl-1H-isochromen-1-one

4-((methyl-d3)thio)-3-phenyl-1H-isochromen-1-one

Conditions
ConditionsYield
With thionyl chloride at 25℃; regioselective reaction;92%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

2-((2-phenyl)ethynyl)-5-methylbenzoic acid methyl ester
1314961-13-1

2-((2-phenyl)ethynyl)-5-methylbenzoic acid methyl ester

7-methyl-4-((methyl-d3)thio)-3-phenyl-1H-isochromen-1-one

7-methyl-4-((methyl-d3)thio)-3-phenyl-1H-isochromen-1-one

Conditions
ConditionsYield
With thionyl chloride at 25℃;91%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

2-[2-(trimethylsilyl)ethynyl]benzoate

2-[2-(trimethylsilyl)ethynyl]benzoate

4-((methyl-d3)thio)-3-(trimethylsilyl)-1H-isochromen-1-one

4-((methyl-d3)thio)-3-(trimethylsilyl)-1H-isochromen-1-one

Conditions
ConditionsYield
With thionyl chloride at 25℃; regioselective reaction;91%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

5-methyl-2-(2-phenylethynyl)benzoate

5-methyl-2-(2-phenylethynyl)benzoate

7-methyl-4-((methyl-d3)thio)-3-phenyl-1H-isochromen-1-one

7-methyl-4-((methyl-d3)thio)-3-phenyl-1H-isochromen-1-one

Conditions
ConditionsYield
With thionyl chloride at 25℃; regioselective reaction;91%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

N,N'-(2,2'-(ethyne-1,2-diyl)bis(2,1-phenylene))bis(4-methylbenzenesulfonamide)
131298-22-1

N,N'-(2,2'-(ethyne-1,2-diyl)bis(2,1-phenylene))bis(4-methylbenzenesulfonamide)

4-methyl-N-(2-(3-((methyl-d3)thio)-1-tosyl-1H-indol-2-yl)phenyl)benzenesulfonamide

4-methyl-N-(2-(3-((methyl-d3)thio)-1-tosyl-1H-indol-2-yl)phenyl)benzenesulfonamide

Conditions
ConditionsYield
With thionyl chloride at 0 - 70℃;91%
With thionyl chloride at 0 - 70℃; for 0.0833333h;91%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

trans-chloro(dimethyl sulfoxide)bis(ethylenediamine)cobalt(III) perchlorate

trans-chloro(dimethyl sulfoxide)bis(ethylenediamine)cobalt(III) perchlorate

trans-[Co(en)2((CD3)2SO)Cl](2+)

trans-[Co(en)2((CD3)2SO)Cl](2+)

cis-[Co(en)2((CD3)2SO)Cl](2+)

cis-[Co(en)2((CD3)2SO)Cl](2+)

Conditions
ConditionsYield
In dimethylsulfoxide-d6 Kinetics; 308.2 K; detected by NMR;A <1
B 90%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

2-(2-(2-thienyl)ethynyl)benzoic acid methyl ester

2-(2-(2-thienyl)ethynyl)benzoic acid methyl ester

4-((methyl-d3)thio)-3-(thiophen-2-yl)-1H-isochromen-1-one

4-((methyl-d3)thio)-3-(thiophen-2-yl)-1H-isochromen-1-one

Conditions
ConditionsYield
With thionyl chloride at 25℃;90%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

2-[2-(thiophen-2-yl)ethynyl]benzoate

2-[2-(thiophen-2-yl)ethynyl]benzoate

4-((methyl-d3)thio)-3-(thiophen-2-yl)-1H-isochromen-1-one

4-((methyl-d3)thio)-3-(thiophen-2-yl)-1H-isochromen-1-one

Conditions
ConditionsYield
With thionyl chloride at 25℃; regioselective reaction;90%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

3,4-dihydronaphthalene-1(2H)-one
529-34-0

3,4-dihydronaphthalene-1(2H)-one

C11H5(2)H3O2S

C11H5(2)H3O2S

Conditions
ConditionsYield
With iodine at 80℃; for 12h; Inert atmosphere;90%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

acetylacetone
123-54-6

acetylacetone

C11H11(2)HO3

C11H11(2)HO3

Conditions
ConditionsYield
With copper(ll) sulfate pentahydrate at 130℃;90%
styrene
292638-84-7

styrene

dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

benzamide
55-21-0

benzamide

C16H13(2)H2NO

C16H13(2)H2NO

Conditions
ConditionsYield
With dipotassium peroxodisulfate; silver(I) acetate; cobalt acetylacetonate at 130℃; for 12h; Mechanism; regioselective reaction;89%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

C23H20N2

C23H20N2

C23H17(2)H3N2

C23H17(2)H3N2

Conditions
ConditionsYield
With potassium tert-butylate at 120℃; for 10h; Inert atmosphere;89%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

C27H23NO

C27H23NO

C27H19(2)H4NO

C27H19(2)H4NO

Conditions
ConditionsYield
With sodium t-butanolate In water-d2 at 75℃; for 24h; Inert atmosphere;88.6%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

4-(methanesulfonyl)acetophenone
10297-73-1

4-(methanesulfonyl)acetophenone

rongalite
149-44-0

rongalite

C20H15(2)H3O6S3

C20H15(2)H3O6S3

Conditions
ConditionsYield
With copper(II) nitrate trihydrate; iodine at 100℃; for 8h;88%
1,1-Diphenylethylene
530-48-3

1,1-Diphenylethylene

dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

deuterated 2-(methylsulfonyl)-1-phenylethanone
1646623-53-1

deuterated 2-(methylsulfonyl)-1-phenylethanone

Conditions
ConditionsYield
With D-Fructose; carbon monoxide; oxygen; copper(II) dipivaloate; palladium dichloride at 80℃; under 760.051 Torr; for 15h;88%
dimethylsulfoxide-d6
2206-27-1

dimethylsulfoxide-d6

2-Nitroanisole
91-23-6

2-Nitroanisole

A

C8H7(2)H2NO3
1304031-30-8

C8H7(2)H2NO3

B

C8H6(2)H3NO3
1304031-27-3

C8H6(2)H3NO3

Conditions
ConditionsYield
With trimethylsulphonium iodide; sodium hydrideA 11.5%
B 87.8%

2206-27-1Relevant articles and documents

A Mechanistic Study of the Reaction of OH with Dimethyl-d6 Sulfide. Direct Observation of Adduct Formation and the Kinetics of the Adduct Reaction with O2

Hynes, A. J.,Stoker, R. B.,Pounds, A. J.,McKay, T.,Bradshaw, J. D.,et al.

, p. 16967 - 16975 (1995)

A pulsed laser photolysis-pulsed laser-induced fluorescence technique has been employed to study the detailed mechanism for the reaction of OH radicals with deuterated dimethyl sulfide .Equilibration of pulsed laser-generated OH with a (CD3)2S-OH adduct has been directly observed, thus confirming the existence of this controversial weakly bound species.Elementary rate coefficients for adduct formation and decomposition and, therefore, the equilibrium constant for OH + (CD3)S (CD3)2SOH have been determined as a function of temperature.From tte temperature dependence of the equilibrium constant over the relatively narrow temperature range 250-267 K, a 258 K adduct bond strength of 13.0 +/- 3.3 kcal mol-1 has been obtained (second law method).Alternatively, an entropy change calculated using standard statistical mechanical methods and ab initio theory (for determining the (CD3)2S and (CD3)2SOH structures) has been employed in conjunction with an experimental value for the equilibrium constant at a single temperature to obtain a 258 K adduct bond strength of 10.1 +/- 1.1 kcal mol-1 (third law method).Experiments in the presence of O2 confirm the previously reported dependence of the OH + DMS-d6 rate coefficient on the O2 partial pressure and are consistent with the previously proposed four-step mechanism involving hydrogen abstraction, addition of OH to the sulfur atom, and adduct decomposition in competition with an adduct + O2 reaction .The rate coefficient for the adduct + O2 reaction is found to be (8 +/-3 ) x 1E-13 cm3 molecule-1 s-1 independent of pressure (100-700 Torr of N2) and temperature (250-300 K).

ULTRAVIOLET RADIATION ABSORBING POLYETHERS

-

Page/Page column, (2014/02/15)

A polymer composition comprising a linear ultraviolet radiation absorbing polyether that comprises a chemically bound UV-chromophore.

POLYARYLENE POLYMERS AND PROCESSES FOR PREPARING

-

, (2012/01/14)

Provided are sulfone-containing polyarylene polymers. Also provided are monomers and processes for preparing the polymers. The polyarylene polymers are suitable for use as engineering polymers.

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