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Cas:96-14-0
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1 Factory price 2 High quality 3 Good service 4 Prompt service Appearance:The crystallization Storage:Kept in dry and cool place and from sunlight; Kept the packing intact. Package: 25kg plastic woven bag with inner linning. Application: Food
J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:96-14-0
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:96-14-0
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inquiryGood quantity Storage:R.T. Package:as per buyers Application:Reagent Transportation:by air/sea
Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
3-METHYLPENTANE Basic information Product Name: 3-METHYLP
Cas:96-14-0
Min.Order:100 Gram
Negotiable
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inquirySprayidea 30 Anti ageing carpet to underlay and upholstery high strength glue Advantages 1.Strong & Permanent bonding,Easy operation; 2.Environment friendly, non-toxic; 3.Large spraying coverage,good elasticity and im
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Min.Order:540 Kilogram
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Type:Other
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The system can just identify the products information in first sheet, it is not be permitted to add or edit new sheet by userself.Our products are required in MG to Gram only. · Pharmaceutical Reference Standards· Traceable workin
Pentane, 3-methyl- Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/Shenzhen
Debyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen
CFTC?PharmaChem?is?a?service?based?company?in?China,?a?pharmachem?division?of?Changzhou?Foreign?Trade?Corp.,supplying?raw?materials,?intermediates,?APIs?and?fine?chemicals?for?the?pharmaceutical?and?specialty?chemical?industries?worldwide. Applicatio
Package:5, 100, 500 mL in glass bottle Application:3-Methylpentane (3MP) is mainly used as a model n-alkane in studies relating to densities, viscosities, refractive indices, excess enthalpies and vapor-liquid equilibrium of binary alkane mixtures.
high purity Application:Drug intermediates Materials intermediates and active molecules
2-vinyl-1,3-butadien
3-methylpentane
Conditions | Yield |
---|---|
With hydrogen; platinum(IV) oxide at 100℃; | 100% |
hydrido(tricarbonyl)(cyclopentadienyl)molybdenum
3-methyl-2-pentene
trifluorormethanesulfonic acid
B
3-methylpentane
Conditions | Yield |
---|---|
In dichloromethane-d2 react. at 22°C for 5 min; detecting by n.m.r. spectroscopy; | A n/a B 100% |
tricarbonylcyclopentadienyltungsten(II) hydride
3-methyl-2-pentene
trifluorormethanesulfonic acid
B
3-methylpentane
Conditions | Yield |
---|---|
In dichloromethane-d2 react. at -80°C for 10 min; detecting by n.m.r. spectroscopy; | A n/a B 100% |
Conditions | Yield |
---|---|
With KL zeolite; potassium chloride; hydrogen; platinum at 469.9℃; under 2250.2 Torr; for 3h; Product distribution; other catalysts; | A n/a B n/a C 88.3% |
With mesoporous silica (MCF-17)/Pt at 360℃; Reagent/catalyst; |
hexane
A
3-methylpentane
B
2-Methylpentane
C
methyl-cyclopentane
D
benzene
Conditions | Yield |
---|---|
at 267.9℃; Product distribution; transformation of n-hexane over Pt black in the presence of hydrogen; effect of the partial pressure of hydrogen and temperature; | A 1.1% B 4.9% C 70.7% D 0.8% E n/a |
C30H74O6Si6
A
hexane
B
3-methylpentane
C
2-Methylpentane
D
2,3-dimethylbutane
Conditions | Yield |
---|---|
With H2SiEt2; [(2,6-[OP(tBu)2]2C6H3)Ir(H)(acetone)]+[B(C6F5)4]- for 336h; Inert atmosphere; Glovebox; | A 45% B 6% C 8% D n/a |
Conditions | Yield |
---|---|
With H2SiEt2; [(2,6-[OP(tBu)2]2C6H3)Ir(H)(acetone)]+[B(C6F5)4]- for 0.333333h; Inert atmosphere; Glovebox; | A 35% B 10% C 13% |
hexane
A
3-methylpentane
B
2-Methylpentane
C
2,2-Dimethylbutane
D
2,3-dimethylbutane
Conditions | Yield |
---|---|
platinum at 250℃; Product distribution; Further Variations:; Catalysts; Temperatures; | A 22.1% B 34.8% C 12.9% D 9% |
With hydrogen at 215℃; under 7500.75 Torr; Catalytic behavior; Kinetics; Reagent/catalyst; Temperature; Flow reactor; Overall yield = 62.1 %; | A n/a B n/a C 6.7% D 8% |
Pt-Al2O3-Cl at 100 - 140℃; under 15001.2 Torr; Product distribution; |
C22H52O5Si4
A
hexane
B
3-methylpentane
C
2-Methylpentane
D
2,3-dimethylbutane
Conditions | Yield |
---|---|
With H2SiEt2; [(2,6-[OP(tBu)2]2C6H3)Ir(H)(acetone)]+[B(C6F5)4]- for 336h; Inert atmosphere; Glovebox; | A 17% B 32% C 31% D n/a |
Conditions | Yield |
---|---|
With H2SiEt2; [(2,6-[OP(tBu)2]2C6H3)Ir(H)(acetone)]+[B(C6F5)4]- for 336h; Inert atmosphere; Glovebox; | A 18% B 29% C 31% |
methanol
A
2,4-dimethylpentane
B
2,3-dimethyl pentane
C
Isobutane
D
methylbutane
E
3-methylpentane
F
2-Methylpentane
G
2,3-dimethylbutane
H
triptane
I
1,2,4,5-tetramethylbenzene
J
1,2,3,5-Tetramethylbenzene
K
pentamethylbenzene,
L
Hexamethylbenzene
Conditions | Yield |
---|---|
With isopropyl alcohol; indium (III) iodide at 200℃; for 2 - 3h; | A n/a B n/a C n/a D n/a E n/a F n/a G n/a H 16.7% I n/a J n/a K n/a L n/a |
2-Methylpentane
A
propane
B
hexane
C
3-methylpentane
D
methyl-cyclopentane
Conditions | Yield |
---|---|
Ir(μ-O-alumina)2(cyclooctadiene)2 at 220℃; Product distribution; variation of catalyst; | A 10.7% B 3.8% C 16.2% D 1.2% |
methylbutane
ethene
A
2,4-dimethylpentane
B
2,5-dimethylhexane
C
2,3-dimethyl pentane
D
2,4-dimethylhexane
E
3-methylpentane
F
2-Methylpentane
Conditions | Yield |
---|---|
boron trifluoride - methanol (1/1) at 35℃; under 7600 Torr; for 1h; Product distribution; oth. catalysts containing BF3, var. ratio of reactants, oth. pressure; | A 14.6% B 6.2% C 13.6% D 3.5% E 4.8% F 15% G n/a |
methanol
A
Isobutane
B
methylbutane
C
3-methylpentane
D
2-Methylpentane
E
2,3-dimethylbutane
F
triptane
G
pentamethylbenzene,
H
Hexamethylbenzene
Conditions | Yield |
---|---|
With isopropyl alcohol; indium (III) iodide at 200℃; for 2 - 3h; Product distribution / selectivity; | A 7.5% B 8.7% C 0.9% D 1.4% E 2.9% F 12.8% G 7.1% H 3.1% |
With hypophosphorous acid; isopropyl alcohol; indium (III) iodide at 200℃; for 2 - 3h; Product distribution / selectivity; | A 10.7% B 10.5% C 1.5% D 2.4% E 2.2% F 9.8% G 3.6% H 1.3% |
methylbutane
ethene
A
2-Methylhexane
B
2,3-dimethyl pentane
C
3-methylpentane
D
2-Methylpentane
E
2,2-Dimethylbutane
F
2,3-dimethylbutane
Conditions | Yield |
---|---|
water; fluorosulphonic acid at -15℃; for 1.5h; Product distribution; | A 5.8% B 6.2% C 8% D n/a E 6.5% F n/a |
methylbutane
A
methane
B
ethane
C
propane
D
Isobutane
E
3-methylpentane
F
2-Methylpentane
Conditions | Yield |
---|---|
With hydrogen; tungsten film at 243.9℃; Product distribution; various temperature, film type, H2-hydrocarbon ratio; | A n/a B n/a C 7.6% D 6.6% E 0.4% F 0.4% |
hexane
A
methylbutane
B
3-methylpentane
C
2-Methylpentane
D
2,2-Dimethylbutane
E
2,3-dimethylbutane
F
pentane
Conditions | Yield |
---|---|
With hydrogen at 180℃; under 11251.1 Torr; for 0.5h; | A 0.6% B n/a C n/a D n/a E n/a F 0.3% |
Conditions | Yield |
---|---|
at 300℃; Erhitzen in Gegenwart von Platin; |
Conditions | Yield |
---|---|
With silicon |
3-iodo-3-methylpentane
3-methylpentane
Conditions | Yield |
---|---|
With zinc copper |
Conditions | Yield |
---|---|
With nickel Hydrogenation; | |
With platinum(IV) oxide Hydrogenation; |
3-methylpentane
Conditions | Yield |
---|---|
With ethanol; zinc |
Conditions | Yield |
---|---|
With nickel Hydrogenation; | |
With platinum(IV) oxide Hydrogenation; | |
Hydrogenation; | |
With CpMo(CO)3H; trifluorormethanesulfonic acid In dichloromethane-d2 at -80℃; for 10h; | 100 % Spectr. |
With hydrogen; ((+)-1,2-bis[(2R,5R)-2,5-diisopropylphospholano]benzene)Co(CO)2H In benzene-d6 at 35℃; under 3040.2 Torr; for 18h; Irradiation; | 50 %Spectr. |
Conditions | Yield |
---|---|
With aluminum tri-bromide; hydrogen bromide |
Conditions | Yield |
---|---|
With aluminum tri-bromide; hydrogen bromide |
2-iodo-3-methyl-pentane
3-methylpentane
Conditions | Yield |
---|---|
With palladium; zinc |
Conditions | Yield |
---|---|
With platinum on activated charcoal at 275 - 320℃; Hydrogenation; | |
With aluminum oxide; nickel at 400℃; Hydrogenation; |
Conditions | Yield |
---|---|
With hydrogen iodide at 210 - 220℃; |
2-ethyl-2-methyl-1,1-diphenyl-butan-1-ol
A
benzophenone
B
3-methylpentane
Conditions | Yield |
---|---|
bei der Destillation; |
Conditions | Yield |
---|---|
With oxygen In benzene at 60℃; under 760.051 Torr; for 1h; Catalytic behavior; Reagent/catalyst; Solvent; | 99% |
With 4-nitroperbenzoic acid In chloroform at 60℃; Rate constant; proportion of velocity of the hydroxylation of tert- and sec. C-H-bonds; | 84% |
With 4-nitroperbenzoic acid In chloroform at 60℃; | 84% |
With lithium aluminium tetrahydride; O(3P) Yield given. Multistep reaction; | |
With tris(μ-oxo)di[(1,4,7-trimethyl-1,4,7-triazanonane)manganese(IV)] hexafluorophosphate; dihydrogen peroxide; acetic acid In acetonitrile at 20℃; for 2h; Product distribution; Mechanism; bond selectivity; |
3-methylpentane
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: CH4; heating of mixt. of Zr(Me)(NHCMe3)((C9H10)2CH2CH2) and C2H5CH(CH3)C2H5 at 75°C for 24 h; | 90% |
Conditions | Yield |
---|---|
With oxygen In dichloromethane at 25℃; under 760.051 Torr; for 2h; | A 90% B 7% |
Conditions | Yield |
---|---|
Stage #1: C14H10ClF3N2O2S With sodium hydride In dichloromethane; mineral oil at 20℃; for 1h; Sealed tube; Stage #2: 3-methylpentane With C26H18Ag2B2Br18N12O2 In dichloromethane; mineral oil at 60℃; for 48h; Sealed tube; Inert atmosphere; regioselective reaction; | 86% |
Conditions | Yield |
---|---|
With Rh2[R-tris(p-tBuC6H4)TPCP]4 In dichloromethane Reflux; enantioselective reaction; | 83% |
Conditions | Yield |
---|---|
With iodosylbenzene In dichloromethane at 25℃; for 2h; Catalytic behavior; Reagent/catalyst; Inert atmosphere; | A 77% B 9% |
Conditions | Yield |
---|---|
With tris(2,2'-bipyridyl)ruthenium dichloride; 4,5,6,7-tetrafluoro-1-hydroxybenzo[d][1,2]iodaoxol-3(1H)-one In dichloromethane at 30℃; Minisci Aromatic Substitution; Inert atmosphere; Irradiation; chemoselective reaction; | 70% |
3-methylpentane
ethyl 2-bromomethyl-2-propenoate
Conditions | Yield |
---|---|
With di-tert-butyl peroxide; potassium carbonate at 130℃; for 8h; Sealed tube; Inert atmosphere; | A 66% B n/a |
Conditions | Yield |
---|---|
With tetrakis[(R)-(1-adamantyl)-(N-phthalimido)acetate]dirhodium(II) In dichloromethane at -40℃; enantioselective reaction; | 64% |
3-methylpentane
A
3-methylpentan-3-ol
B
3-methyl-pentan-2-one
C
3-Methyl-2,4-pentanedione
Conditions | Yield |
---|---|
With iodosylbenzene In dichloromethane at 25℃; for 2h; Catalytic behavior; Solvent; Reagent/catalyst; Inert atmosphere; | A 61% B 7% C 28% |
3-methylpentane
A
3-methylpentan-2-ol
B
3-methylpentan-3-ol
C
3-methyl-pentan-2-one
Conditions | Yield |
---|---|
With iodosylbenzene In dichloromethane at 25℃; for 3h; Solvent; Inert atmosphere; | A 10% B 60% C 18% |
3-methylpentane
A
tetradecafluorohexane
B
perfluoroisohexane
C
perfluoro(3-methylpentane)
D
perfluoro(2-methylcyclopentane)
Conditions | Yield |
---|---|
cobalt (III) fluoride at 360℃; for 3h; Further byproducts given; | A 7% B 9% C 57% D 21% |
3-methylpentane
A
tetradecafluorohexane
B
perfluoroisohexane
C
perfluoro(3-methylpentane)
D
perfluoro(2-methylcyclopentane)
E
perfluoro(2,2-dimethylbutane)
Conditions | Yield |
---|---|
cobalt (III) fluoride at 360℃; for 3h; Product distribution; | A 7% B 9% C 57% D 21% E 1% |
3-methylpentane
A
3-methylpentan-2-ol
B
3-methyl-1-pentanol
C
3-methylpentan-3-ol
D
3-methyl-pentan-2-one
Conditions | Yield |
---|---|
With iodosylbenzene In dichloromethane at 25℃; for 2h; Inert atmosphere; | A 14% B 12% C 57% D 13% |
With iodosylbenzene In dichloromethane at 25℃; for 2h; Inert atmosphere; | A 11% B 24% C 52% D 6% |
Conditions | Yield |
---|---|
With O(3P) Product distribution; | A 52% B n/a |
3-methylpentane
[(3-bromoprop-1-en-2-yl)sulfonyl]benzene
Conditions | Yield |
---|---|
With di-tert-butyl peroxide; potassium carbonate at 130℃; for 8h; Sealed tube; Inert atmosphere; | A 48% B n/a |
3-methylpentane
1,1,3,3-tetramethyl-2,3-dihydro-1H-isoindol-2-yloxoyl radical
Conditions | Yield |
---|---|
With di-tert-butyl diperoxyoxalate at 60℃; for 1.16667h; Further byproducts given; | A 44.3% B 3.1% C 41.7% D 7.8% |
3-methylpentane
methyl 2-isocyano-3,3-diphenyl acrylate
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene; dibenzoyl peroxide at 100℃; for 2h; Sealed tube; Inert atmosphere; Overall yield = 51 %; | A 17% B 34% |
3-methylpentane
α-(bromomethyl)acrylonitrile
Conditions | Yield |
---|---|
With di-tert-butyl peroxide; potassium carbonate at 130℃; for 8h; Sealed tube; Inert atmosphere; | A 28% B n/a |
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