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Supplier: Thermo Scientific Chemicals
Description: Allyl alcohol 99%, Extra Pure

Catalog Number: (AAA-15026-AP)
Supplier: Thermo Scientific Chemicals

Catalog Number: (RK30214)
Supplier: Restek
Description: Mix contains: Allyl alcohol (2-propen-1-ol) (107-18-6); 2-Chloroethanol (107-07-3); Ethanol (64-17-5); Isobutyl alcohol (78-83-1); Propargyl alcohol (107-19-7).


Supplier: Thermo Scientific Chemicals
Description: 2-Methyl-2-propen-1-ol 98%

Supplier: ALADDIN SCIENTIFIC CORPORATION
Description: Allyltrimethoxysilane is an allylating reagent that can be used for the allylation of carbonyl compounds such as aldehydes, ketones, and imines. Homoallylic alcohols and amines are obtained via the C-C bond forming reaction.It can also be used to synthesize homoallylic α-branched amines from aromatic and aliphatic aldehyde hydrazones, and ketone hydrazones.

New Product

Catalog Number: (76473-392)
Supplier: BTNX INC.
Description: The Rapid Response® Alcohol test strip is a rapid and highly sensitive method to detect the presence of alcohol in saliva to provide an approximation of relative blood alcohol concentration (BAC) at 0.02% or greater.


Catalog Number: (AAH60502-06)
Supplier: Thermo Scientific Chemicals
Description: 2-Methyl-2-propen-1-ol, Purity: 98%, CAS Number: 513-42-8, Molecular Formula: C4H8O, Color: Colourless, Form: Liquid, Synonym: beta-Methallyl alcohol, Size: 5G

Supplier: ALADDIN SCIENTIFIC CORPORATION
Description: Aldehyde allylation reagent, the catalyst of this reaction is chiral Lewis acid and Ytterbium(III) trifluoromethanesulfonate. Catalyzed by tetrakis(triphenylphosphine)palladium (0) (product number 216666), it reacts with iodoquinone 4 and allyl acetate. Used in the efficient allylation reaction of aldehydes and trichloro-1,3,5-triazene to produce high allyl alcohol.

New Product

Supplier: TCI America
Description: CAS Number: 513-42-8
MDL Number: MFCD00004737
Molecular Formula: C4H8O
Molecular Weight: 72.11
Purity/Analysis Method: >98.0% (GC)
Form: Clear Liquid
Boiling point (°C): 113
Flash Point (°C): 33
Specific Gravity (20/20): 0.85
Supplier: Thermo Scientific Chemicals
Description: Manganese(IV) oxide is suitable for use in batteries. It is widely used for the selective oxidation of allylic and benzylic alcohols to aldehydes or ketones, as a co-oxidant in combination with 1,4-benzoquinone and in the allylic oxidation of olefins catalyzed by Palladium(II)­ acetate. It acts a reagent for oxidations. It is the source of manganese and all its compounds, largely used in manufacturing of manganese steel, for making amethyst glass, decolorizing glass, painting on porcelain, faience and majolica. The precipitate is used in electrotechnics, pigments, browning gun barrels, drier for paints and varnishes, printing and dyeing textiles.
Supplier: ALADDIN SCIENTIFIC CORPORATION
Description: Product classM-P, Homogeneous Catalysts, N-Heterocyclic Carbene Ligands, M-C, Allyl Ligands, SIPr, Bidentate LigandsReaction typeCross Coupling Reactions with Arenes, Amination, Buchwald-Hartwig Aminaton, Alpha Arylation, Suzuki-Miyaura Coupling ReactionChemical propertiesChemical formulaC30H43N2ClPdEmpirical formula(SIPr)Pd(allyl)ClMolecular weight573.56MetalPdTheoretical metal content19Physical statecrystallineColoryellowMetal purity99.95Applications & referencesα-Arylation of ketones.Reference: Org. Lett. 2002, 4, 4053 (DOI: 10.1021/ol026745m); Adv. Synth. Catal. 2012, 354, 377 (DOI: 10.1002/adsc.201100669)Intramolecular arylamination step in the synthetic approach of cryptocarya alkaloids.Reference: Synlett 2003, 12, 1871 (DOI: 10.1021/jo035834p)Suzuki-Miyaura coupling reaction.Reference: J. Org. Chem. 2004, 69, 3173Buchwald-Hartwig coupling reactions.Reference: J. Am. Chem. Soc. 2006, 128, 4101 (DOI: 10.1021/ja057704z)α-Heteroarylation of ketone enolates.Reference: J. Org. Chem. 2010, 75, 5316 (DOI: 10.1021/jo100623d)Palladium catalyzed anaerobic oxidation of secondary alcohols under mild reaction conditions.Reference: J. Org. Chem. 2011, 76, 1390. (DOI: 10.1021/jo102385u)Palladium catalyzed Buchwald-Hartwig- Reaction at room temperature.Reference: J. Am. Chem. Soc. 2006, 128, 4101. (DOI: 10.10217ja057704z)

New Product

Catalog Number: (75835-544)
Supplier: Restek
Description: The mix consists of acetonitrile, acrylonitrile, allyl chloride , benzene, bromobenzene, bromochloromethane, bromodichloromethane, bromoform, n-butylbenzene, sec-butylbenzene, tert-butylbenzene, carbon disulfide, carbon tetrachloride, chlorobenzene, 2-chloroethanol, chloroform, chloroprene , 2-chlorotoluene, 4-chlorotoluene, dibromochloromethane, 1,2-dibromo-3-chloropropane , 1,2-dibromoethane , dibromomethane, 1,2-dichlorobenzene, 1,3-dichlorobenzene, 1,4-dichlorobenzene, cis-1,4-dichloro-2-butene, trans-1,4-dichloro-2-butene, 1,1-dichloroethane, 1,2-dichloroethane, 1,1-dichloroethene, cis-1,2-dichloroethene, trans-1,2-dichloroethene, 1,2-dichloropropane, 1,3-dichloropropane, 2,2-dichloropropane, 1,1-dichloropropene, cis-1,3-dichloropropene, trans-1,3-dichloropropene, diethyl ether , 1,4-dioxane, ethylbenzene, ethyl methacrylate, hexachloro-1,3-butadiene, iodomethane , isobutyl alcohol , isopropylbenzene , 4-isopropyl toluene , methacrylonitrile, methyl acrylate, methyl methacrylate, methylene chloride , naphthalene, nitrobenzene, 2-nitropropane, propionitrile, n-propylbenzene, styrene, 1,1,1,2-tetrachloroethane, 1,1,2,2-tetrachloroethane, tetrachloroethene, tetrahydrofuran, toluene, 1,2,3-trichlorobenzene, 1,1,1-trichloroethane, 1,1,2-trichloroethane, trichloroethene, 1,2,3-trichloropropane, 1,1,2-trichlorotrifluororethane , 1,2,4-trimethylbenzene, 1,3,5-trimethylbenzene, m-xylene, o-xylene, p-xylene.


Catalog Number: (75831-174)
Supplier: Restek
Description: Contains: Acetonitrile (75-05-8); Acrylonitrile (107-13-1); Allyl chloride (3-chloropropene) (107-05-1); Benzene (71-43-2); Bromobenzene (108-86-1); Bromochloromethane (74-97-5); Bromodichloromethane (75-27-4); Bromoform (75-25-2); n-Butylbenzene (104-51-8); sec-Butylbenzene (135-98-8); tert-Butylbenzene (98-06-6); Carbon disulfide (75-15-0); Carbon tetrachloride (56-23-5); Chlorobenzene (108-90-7); 2-Chloroethanol (107-07-3); Chloroform (67-66-3); Chloroprene (2-chloro-1,3-butadiene) (126-99-8); 2-Chlorotoluene (95-49-8); 4-Chlorotoluene (106-43-4); Dibromochloromethane (124-48-1); 1,2-Dibromo-3-chloropropane (DBCP) (96-12-8); 1,2-Dibromoethane (EDB) (106-93-4); Dibromomethane (74-95-3); 1,2-Dichlorobenzene (95-50-1); 1,3-Dichlorobenzene (541-73-1); 1,4-Dichlorobenzene (106-46-7); cis-1,4-Dichloro-2-butene (1476-11-5); trans-1,4-Dichloro-2-butene (110-57-6); 1,1-Dichloroethane (75-34-3); 1,2-Dichloroethane (107-06-2); 1,1-Dichloroethene (75-35-4); cis-1,2-Dichloroethene (156-59-2); trans-1,2-Dichloroethene (156-60-5); 1,2-Dichloropropane (78-87-5); 1,3-Dichloropropane (142-28-9); 2,2-Dichloropropane (594-20-7); 1,1-Dichloropropene (563-58-6); cis-1,3-Dichloropropene (10061-01-5); trans-1,3-Dichloropropene (10061-02-6); Diethyl ether (ethyl ether) (60-29-7); 1,4-Dioxane (123-91-1); Ethylbenzene (100-41-4); Ethyl methacrylate (97-63-2); Hexachloro-1,3-butadiene (87-68-3); Iodomethane (methyl iodide) (74-88-4); Isobutyl alcohol (2-methyl-1-propanol) (78-83-1); Isopropylbenzene (cumene) (98-82-8); 4-Isopropyl toluene (p-Cymene) (99-87-6); Methacrylonitrile (126-98-7); Methyl acrylate (96-33-3); Methyl methacrylate (80-62-6); Methylene chloride (dichloromethane) (75-09-2); Naphthalene (91-20-3); Nitrobenzene (98-95-3); 2-Nitropropane (79-46-9); Pentachloroethane (76-01-7); Propionitrile (107-12-0); n-Propylbenzene (103-65-1); Styrene (100-42-5); 1,1,1,2-Tetrachloroethane (630-20-6); 1,1,2,2-Tetrachloroethane (79-34-5); Tetrachloroethene (127-18-4); Tetrahydrofuran (109-99-9); Toluene (108-88-3); 1,2,3-Trichlorobenzene (87-61-6); 1,2,4-Trichlorobenzene (120-82-1); 1,1,1-Trichloroethane (71-55-6); 1,1,2-Trichloroethane (79-00-5); Trichloroethene (79-01-6); 1,2,3-Trichloropropane (96-18-4); 1,1,2-Trichlorotrifluoroethane (CFC-113) (76-13-1); 1,2,4-Trimethylbenzene (95-63-6); 1,3,5-Trimethylbenzene (108-67-8); m-Xylene (108-38-3); o-Xylene (95-47-6); p-Xylene (106-42-3)


Supplier: Thermo Scientific Chemicals
Description: Dess Martin periodinane is used to oxidize primary alcohols to aldehydes and secondary alcohols to ketones. It is also used as an oxidant for complexes with multifunctional alcohols. It is actively involved in the oxidation of N-protected-amino alcohols without epimerization and allylic alcohols.
Supplier: Ambeed
Description: 2-Allyl-D-glycine 97%

New Product

Catalog Number: (TCA2679-25ML)
Supplier: TCI America
Description: CAS Number: 7493-72-3
MDL Number: MFCD00038344
Molecular Formula: C12H22O2
Molecular Weight: 198.31
Purity/Analysis Method: >97.0% (GC)
Form: Clear Liquid
Boiling point (°C): 151
Specific Gravity (20/20): 0.88

SDS


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