115-18-4 | 3-Buten-2-ol, 2-methyl-

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$25.00	$18.00
25g	98%	in stock	$42.00	$30.00
100g	98%	in stock	$90.00	$63.00
500g	98%	in stock	$251.00	$176.00

Description

• Catalog Number: AA19957
• Chemical Name: 3-Buten-2-ol, 2-methyl-
• CAS Number: 115-18-4
• Molecular Formula: C5H10O
• Molecular Weight: 86.1323
• MDL Number: MFCD00004470
• SMILES: C=CC(O)(C)C
• NSC Number: 15977

Computed Properties

• Complexity: 55
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 6
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 0.8

Upstream Synthesis Route

2-Methyl-3-buten-2-ol is a versatile compound commonly used in chemical synthesis for its valuable properties. As a primary alcohol, it serves as a crucial building block in the production of various chemical products. Its unique structure consisting of a double bond and a methyl group provides opportunities for diverse functionalization in organic synthesis. In particular, 2-Methyl-3-buten-2-ol is utilized in the synthesis of pharmaceutical compounds, agrochemicals, and fragrances. Its reactivity allows for the introduction of different functional groups, enabling the creation of complex molecules with specific applications. Additionally, its presence in the synthesis of flavor compounds highlights its significance in the food and beverage industry. With its role in creating a wide range of compounds, 2-Methyl-3-buten-2-ol proves to be an indispensable component in chemical synthesis.

Literature

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  Environmental science & technology 20120904

• The sedative effects of hops (Humulus lupulus), a component of beer, on the activity/rest rhythm.

  Acta physiologica Hungarica 20120601

• Improved lycopene production by Blakeslea trispora with isopentenyl compounds and metabolic precursors.

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• Identification, functional characterization, and regulation of the enzyme responsible for floral (E)-nerolidol biosynthesis in kiwifruit (Actinidia chinensis).

  Journal of experimental botany 20120301

• Bacterial degradation of tert-amyl alcohol proceeds via hemiterpene 2-methyl-3-buten-2-ol by employing the tertiary alcohol desaturase function of the Rieske nonheme mononuclear iron oxygenase MdpJ.

  Journal of bacteriology 20120301

• The sedative effect of non-alcoholic beer in healthy female nurses.

  PloS one 20120101

• [Uptake of 3-methyl-3-buten-1-ol into aqueous mixed solution of sulfuric acid and hydrogen peroxide].

  Huan jing ke xue= Huanjing kexue 20111201

• Host resistance elicited by methyl jasmonate reduces emission of aggregation pheromones by the spruce bark beetle, Ips typographus.

  Oecologia 20111101

• Palladium-catalyzed mono-N-allylation of unprotected anthranilic acids with allylic alcohols in aqueous media.

  The Journal of organic chemistry 20111021

• Efficient discovery of potent anti-HIV agents targeting the Tyr181Cys variant of HIV reverse transcriptase.

  Journal of the American Chemical Society 20111005

• Structure sensitivity of alkynol hydrogenation on shape- and size-controlled palladium nanocrystals: which sites are most active and selective?

  Journal of the American Chemical Society 20110817

• Attraction modulated by spacing of pheromone components and anti-attractants in a bark beetle and a moth.

  Journal of chemical ecology 20110801

• Biochemical characterization and homology modeling of methylbutenol synthase and implications for understanding hemiterpene synthase evolution in plants.

  The Journal of biological chemistry 20110610

• Palladium-catalyzed mono-N-allylation of unprotected amino acids with 1,1-dimethylallyl alcohol in water.

  Organic & biomolecular chemistry 20110607

• The uptake of 2-methyl-3-buten-2-ol into aqueous mixed solutions of sulfuric acid and hydrogen peroxide.

  Physical chemistry chemical physics : PCCP 20110214

• Dietary essential amino acids affect the reproduction of the keystone herbivore Daphnia pulex.

  PloS one 20110101

• Identification and field activity of a male-produced aggregation pheromone in the pine sawyer beetle, Monochamus galloprovincialis.

  Journal of chemical ecology 20100601

• Kinetics and mechanism of chlorine-atom-initiated oxidation of allyl alcohol, 3-buten-2-ol, and 2-methyl-3-buten-2-ol.

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• Fragrance material review on 2-methyl-3-buten-2-ol.

  Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 20100101

• Gene expression and activity of digestive proteases in Daphnia: effects of cyanobacterial protease inhibitors.

  BMC physiology 20100101

• Inhibition of predator attraction to kairomones by non-host plant volatiles for herbivores: a bypass-trophic signal.

  PloS one 20100101

• Photooxidation of 2-methyl-3-Buten-2-ol (MBO) as a potential source of secondary organic aerosol.

  Environmental science & technology 20090701

• Specificity and redundancy in the olfactory system of the bark beetle Ips typographus: single-cell responses to ecologically relevant odors.

  Journal of insect physiology 20090601

• Aggregation pheromone of the Qinghai spruce bark beetle, Ips nitidus eggers.

  Journal of chemical ecology 20090501

• Target gene approaches: Gene expression in Daphnia magna exposed to predator-borne kairomones or to microcystin-producing and microcystin-free Microcystis aeruginosa.

  BMC genomics 20090101

• Metasternal gland volatiles and sexual communication in the triatomine bug, Rhodnius prolixus.

  Journal of chemical ecology 20080401

• Electrophysiological and behavioral responses of Ips duplicatus to aggregation pheromone in Inner Mongolia, China: amitinol as a potential pheromone component.

  Journal of chemical ecology 20070701

• Biosynthesis, accumulation and emission of carotenoids, alpha-tocopherol, plastoquinone, and isoprene in leaves under high photosynthetic irradiance.

  Photosynthesis research 20070501

• Experimental and theoretical studies of the kinetics of the reactions of OH and OD with 2-methyl-3-buten-2-ol between 300 and 415 K at low pressure.

  The journal of physical chemistry. A 20070201

• The uptake of methyl vinyl ketone, methacrolein, and 2-methyl-3-butene-2-ol onto sulfuric acid solutions.

  The journal of physical chemistry. A 20060223

• Peroxy and alkoxy radicals from 2-methyl-3-buten-2-ol.

  Physical chemistry chemical physics : PCCP 20060128

• Hydroxyaldehyde products from hydroxyl radical reactions of Z-3-hexen-1-ol and 2-methyl-3-buten-2-ol quantified by SPME and API-MS.

  Environmental science & technology 20031015

• Chemical composition of the essential oils of two Rhodiola species from Tibet.

  Zeitschrift fur Naturforschung. C, Journal of biosciences 20030101

• Field response of Ips paraconfusus, Dendroctonus brevicomis, and their predators to 2-methyl-3-buten-2-ol, a novel alcohol emitted by ponderosa pine.

  Journal of chemical ecology 20020801

• Differential accumulation of dimethylallyl diphosphate in leaves and needles of isoprene- and methylbutenol-emitting and nonemitting species.

  Plant physiology 20020701

• Ion trap mass spectrometry affords advances in the analytical and atmospheric chemistry of 2-hydroxy-2-methylpropanal, a proposed photooxidation product of 2-methyl-3-buten-2-Ol.

  Journal of the American Society for Mass Spectrometry 20020501

• Volatile components in aqueous essence and fresh fruit of Cucumis melo cv. Athena (muskmelon) by GC-MS and GC-O.

  Journal of agricultural and food chemistry 20011201

• Dose-dependent response and preliminary observations on attraction range of Ips typographus to pheromones at low release rates.

  Journal of chemical ecology 20011201

• Biosynthesis of 2-methyl-3-buten-2-ol emitted from needles of Pinus ponderosa via the non-mevalonate DOXP/MEP pathway of isoprenoid formation.

  Planta 20010601

• Synthesis of farnesyl diphosphate analogues containing ether-linked photoactive benzophenones and their application in studies of protein prenyltransferases.

  The Journal of organic chemistry 20010518

• Canopy level fluxes of 2-methyl-3-buten-2-ol, acetone, and methanol by a portable relaxed eddy accumulation system.

  Environmental science & technology 20010501

• Enzymatic synthesis of methylbutenol from dimethylallyl diphosphate in needles of Pinus sabiniana.

  Archives of biochemistry and biophysics 20001101