821-09-0 | 4-Penten-1-ol

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$12.00	$8.00
10g	98%	in stock	$15.00	$10.00
25g	98%	in stock	$18.00	$12.00
100g	98%	in stock	$56.00	$39.00

Description

• Catalog Number: AC28488
• Chemical Name: 4-Penten-1-ol
• CAS Number: 821-09-0
• Molecular Formula: C5H10O
• Molecular Weight: 86.1323
• MDL Number: MFCD00002975
• SMILES: OCCCC=C
• NSC Number: 97503

Computed Properties

• Complexity: 32.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 6
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 1

Literature

• Retrograde signaling by the plastidial metabolite MEcPP regulates expression of nuclear stress-response genes.

  Cell 20120622

• Molecular cloning and functional characterization of Catharanthus roseus hydroxymethylbutenyl 4-diphosphate synthase gene promoter from the methyl erythritol phosphate pathway.

  Molecular biology reports 20120501

• Proteomic analysis of papaya fruit ripening using 2DE-DIGE.

  Journal of proteomics 20120202

• Maize provitamin a carotenoids, current resources, and future metabolic engineering challenges.

  Frontiers in plant science 20120101

• A proteomic analysis of the chromoplasts isolated from sweet orange fruits [Citrus sinensis (L.) Osbeck].

  Journal of experimental botany 20111101

• An ENDOR and HYSCORE investigation of a reaction intermediate in IspG (GcpE) catalysis.

  Journal of the American Chemical Society 20110608

• Mechanistic investigation of the base-promoted cycloselenoetherification of pent-4-en-1-ol.

  Journal of molecular modeling 20110601

• Structure of the E-1-hydroxy-2-methyl-but-2-enyl-4-diphosphate synthase (GcpE) from Thermus thermophilus.

  FEBS letters 20110204

• The methylerythritol phosphate (MEP) pathway for isoprenoid biosynthesis as a target for the development of new drugs against tuberculosis.

  Current medicinal chemistry 20110101

• Characterization of 1-hydroxy-2-methyl-2-(E)-butenyl-4-diphosphate synthase (HDS) gene from Ginkgo biloba.

  Molecular biology reports 20100201

• Strictosidine activation in Apocynaceae: towards a 'nuclear time bomb'?

  BMC plant biology 20100101

• Optimization of the transient transformation of Catharanthus roseus cells by particle bombardment and its application to the subcellular localization of hydroxymethylbutenyl 4-diphosphate synthase and geraniol 10-hydroxylase.

  Plant cell reports 20090801

• Comparative transcripts profiling reveals new insight into molecular processes regulating lycopene accumulation in a sweet orange (Citrus sinensis) red-flesh mutant.

  BMC genomics 20090101

• Isomer-specific influences on the composition of reaction intermediates in dimethyl ether/propene and ethanol/propene flame.

  The journal of physical chemistry. A 20081002

• Contribution of hydroxymethylbutenyl diphosphate synthase to carotenoid biosynthesis in bacteria and plants.

  Biochemical and biophysical research communications 20080704

• Highly efficient asymmetric synthesis of fluvirucinine A1 via Zr-catalyzed asymmetric carboalumination of alkenes (ZACA)-lipase-catalyzed acetylation tandem process.

  Organic letters 20080117

• Spatial distribution and hormonal regulation of gene products from methyl erythritol phosphate and monoterpene-secoiridoid pathways in Catharanthus roseus.

  Plant molecular biology 20070901

• Possible direct involvement of the active-site [4Fe-4S] cluster of the GcpE enzyme from Thermus thermophilus in the conversion of MEcPP.

  FEBS letters 20070123

• Characterizing ionic liquids as reaction media through a chemical probe.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20070101

• On the stereoselectivity of 4-penten-1-oxyl radical 5-exo-trig cyclizations.

  Organic & biomolecular chemistry 20061121

• Asymmetric synthesis of anti-1,2-amino alcohols via the Borono-Mannich reaction: a formal synthesis of (-)-swainsonine.

  The Journal of organic chemistry 20060901

• Precise investigation of the axial ligand substitution mechanism on a hydrogenphosphato-bridged lantern-type platinum(III) binuclear complex in acidic aqueous solution.

  Inorganic chemistry 20051031

• The Arabidopsis csb3 mutant reveals a regulatory link between salicylic acid-mediated disease resistance and the methyl-erythritol 4-phosphate pathway.

  The Plant journal : for cell and molecular biology 20051001

• Cyanobacterial non-mevalonate pathway: (E)-4-hydroxy-3-methylbut-2-enyl diphosphate synthase interacts with ferredoxin in Thermosynechococcus elongatus BP-1.

  The Journal of biological chemistry 20050527

• Synthesis of unsaturated amino alcohols through unexpectedly selective Ru-catalyzed cross-metathesis reactions.

  Organic letters 20050526

• Alpha-N-acetylmannosamine (ManNAc) synthesis via rhodium(II)-catalyzed oxidative cyclization of glucal 3-carbamates.

  The Journal of organic chemistry 20050513

• On the 6-endo selectivity in 4-penten-1-oxyl radical cyclizations.

  Journal of the American Chemical Society 20040929

• Mechanism of the axial ligand substitution reactions on the head-to-tail alpha-pyridonato-bridged cis-diammineplatinum(III) dinuclear complex with olefins.

  Inorganic chemistry 20040112

• Glycosynthase-catalysed syntheses at pH below neutrality.

  Bioorganic & medicinal chemistry letters 20031117

• A genetic basis for human gammadelta T-cell reactivity towards microbial pathogens.

  Trends in immunology 20030801

• Bioinformatic and molecular analysis of hydroxymethylbutenyl diphosphate synthase (GCPE) gene expression during carotenoid accumulation in ripening tomato fruit.

  Planta 20030701

• Mechanism of ketone and alcohol formations from alkenes and alkynes on the head-to-head 2-pyridonato-bridged cis-diammineplatinum(III) dinuclear complex.

  Journal of the American Chemical Society 20030326

• Functional characterization of GcpE, an essential enzyme of the non-mevalonate pathway of isoprenoid biosynthesis.

  FEBS letters 20021218

• Isoprenoid biosynthesis through the methylerythritol phosphate pathway: the (E)-4-hydroxy-3-methylbut-2-enyl diphosphate synthase (GcpE) is a [4Fe-4S] protein.

  Angewandte Chemie (International ed. in English) 20021115

• Biosynthesis of terpenes. Preparation of (E)-1-hydroxy-2-methyl-but-2-enyl 4-diphosphate, an intermediate of the deoxyxylulose phosphate pathway.

  The Journal of organic chemistry 20020628

• Identification of (E)-4-hydroxy-3-methyl-but-2-enyl pyrophosphate as a major activator for human gammadelta T cells in Escherichia coli.

  FEBS letters 20011207

• Cutting edge: human gamma delta T cells are activated by intermediates of the 2-C-methyl-D-erythritol 4-phosphate pathway of isoprenoid biosynthesis.

  Journal of immunology (Baltimore, Md. : 1950) 20010315

• Identification of gcpE as a novel gene of the 2-C-methyl-D-erythritol 4-phosphate pathway for isoprenoid biosynthesis in Escherichia coli.

  FEBS letters 20010119