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Valeraldehyde | CAS:110-62-3
Valeraldehyde
  • 名称:戊醛; 正戊醛 | Valeraldehyde
  • CAS号:110-62-3
  • 别名:Pentanal; Valeral; Valeric aldehyde
  • 分子式:C5H10O
  • 分子量:86.13
  • EINESC号:203-784-4

产品描述

物理化学性质

熔点 -92 ºC
水溶性 14 g/L (20 ºC)
沸点 103 ºC
闪点 12 ºC
密度 0.807
折射率 1.39-1.395

安全数据

危险品标志 F;Xi
危险类别码 R11;R36/37/38
安全说明书 S16;S26;S37/39

SDS

来源 SDS样本
没有数据没有数据
产品合成路线
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Desaturation, dioxygenation, and monooxygenation reactions catalyzed by naphthalene dioxygenase from Pseudomonas sp. strain 9816-4.D T Gibson et al.Journal of bacteriology, 177(10), 2615-2621 (1995-05-01) Aromatic hydroxylation of indan by o-xylene-degrading Rhodococcus sp. strain DK17.Dockyu Kim et al.Applied and environmental microbiology, 76(1), 375-377 (2009-11-03) Kinetic resolutions of indan derivatives using bacteria.Naoki Tarui et al.Bioscience, biotechnology, and biochemistry, 66(2), 464-466 (2002-05-10) Hypolipidemic activity of Indan--1--acetic acids.Manoranjan Adak et al.Nepal Medical College journal : NMCJ, 8(1), 22-26 (2006-07-11) Stereochemical control of the Passerini reaction.Peter R Andreana et al.Organic letters, 6(23), 4231-4233 (2004-11-05) Preparation of alkylidene indane and related scaffolds and their further elaboration to novel chemotypes.Sarathy Kesavan et al.Organic letters, 9(25), 5203-5206 (2007-11-14) Asymmetric hydrogenation of ketones catalyzed by a ruthenium(II)-indan-ambox complex.Wei Li et al.Chemical communications (Cambridge, England), 46(22), 3979-3981 (2010-04-22) Predictive three-dimensional quantitative structure-activity relationship of cytochrome P450 1A2 inhibitors.Laura E Korhonen et al.Journal of medicinal chemistry, 48(11), 3808-3815 (2005-05-27) Simultaneous determination of ethylbenzene, indan, indene and acenaphthene in air by capillary gas chromatography.G Bieniek Journal of chromatography. A, 891(2), 361-365 (2000-10-24) Selective inhibition of carboxylesterases by isatins, indole-2,3-diones.Janice L Hyatt et al.Journal of medicinal chemistry, 50(8), 1876-1885 (2007-03-24) Highly efficient biocatalytic resolution of cis- and trans-3-aminoindan-1-ol: syntheses of enantiopure orthogonally protected cis- and trans-indane-1,3-diamine.Mónica López-García et al.Chemistry (Weinheim an der Bergstrasse, Germany), 10(12), 3006-3014 (2004-06-24) (1S)-1-Phenylethanaminium 4-{[(1S,2S)-1-hydroxy-2,3-dihydro-1H,1'H-[2,2'-biinden]-2-yl]methyl}benzoate.Christopher S Frampton et al.Acta crystallographica. Section C, Crystal structure communications, 68(Pt 8), o323-o326 (2012-08-02) A new NF-kappaB inhibitor attenuates a TH1 type immune response in a murine model.Kenji Kabashima et al.FEBS letters, 578(1-2), 36-40 (2004-12-08) Bicyclic naphthenic acids in oil sands process water: identification by comprehensive multidimensional gas chromatography-mass spectrometry.Michael J Wilde et al.Journal of chromatography. A, 1378, 74-87 (2015-01-03) Aryl sulfonamido indane inhibitors of the Kv1.5 ion channel.Michael F Gross et al.Bioorganic & medicinal chemistry letters, 17(10), 2849-2853 (2007-03-14) Discovery of a series of indan carboxylic acid glycogen phosphorylase inhibitors.Stuart N L Bennett et al.Bioorganic & medicinal chemistry letters, 20(12), 3511-3514 (2010-05-25) Screening for petrochemical contamination in seafood by headspace solid-phase microextraction gas chromatography-mass spectrometry.F Aladar Bencsath et al.Analytical and bioanalytical chemistry, 407(14), 4079-4090 (2015-03-23) Synthesis of [60]fullerene-fused tetrahydronaphthalene and indane derivatives via a pathway switched by aluminum chloride.Tong-Xin Liu et al.Organic letters, 13(22), 6130-6133 (2011-10-29) Conformationally constrained analogues of N'-(4-tert-butylbenzyl)-N-(4-methylsulfonylaminobenzyl)thiourea as TRPV1 antagonists.Ju-Ok Lim et al.European journal of medicinal chemistry, 44(1), 322-331 (2008-04-15) Synthesis, absolute configuration, and application of enantiopure trans-1-aminobenz[f]indan-2-ol.Yuka Kobayashi et al.Chirality, 17(2), 108-112 (2005-01-22) Novel 5-dimethylamino-1- and 2-indanyl uracil derivatives.Konstantin Ulanenko et al.The Journal of organic chemistry, 71(18), 7053-7056 (2006-08-26)
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