英文名称: 2-furylmethanol CAS No.: 93793-62-5 分子式: C5H6O2 分子量: 98.0999417304993 如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:2-furylmethanol结构式 下载该化合物MOL文件: 2-furylmethanolMOL 快速询单 2-furylmethanol的其他展现形式 相关化合物 呋喃树脂 2-Furanmethanol, homop...
Tetrahydro-2-Furylmethanol 97-99-4doi:10.1002/0471701343.sdp23666This article has no abstract.John Wiley & Sons, Inc.Sax's Dangerous Properties of Industrial Materials
中文名:2,2'-DIFURYLMETHANOL,英文名:2,2'-DIFURYLMETHANOL,CAS:,化学式:C9H8O3,分子量:164.16,MSDS.
M. D'Auria, L. Emanuele, G. Poggi, R. Racioppi, G. Romanielli, On the stereoselectivity of the Paterno-Buchi reaction between carbonyl compounds and 2-furylmethanol derivatives: the case of aliphatic aldehydes and ketones, Tetrahedron 58 (2002) 5045-5051....
别名(5-甲基四氢呋喃-2-基)甲醇 | 四氢-5-甲基-2-呋喃甲醇 英文别名5-(Hydroxymethyl)tetrahydro-2-furanol | 2-Furanmethanol, tetrahydro-5-methyl- | EN300-120684 | cis-(5-Methyltetrahydrofuran-2-yl)methanol | (5-methyl-tetrahydro-furan-2-yl)-methanol | (5-Methyltetrahydrofuran-2-yl)methanol...
2,3'-DIFURYLMETHANOL CAS号: 英文名: 2,3'-DIFURYLMETHANOL 英文别名: 2,3'-DIFURYLMETHANOL 中文名: 中文别名: CBNumber: CB5392957 分子式: C9H8O3 分子量: 164.16 MOL File: Mol file 化学性质 安全信息 用途 供应商 1 2,3'-DIFURYLMETHANOL化学性质 ...
2,2'-DIFURYLMETHANOL 推荐供应商 建议您优先选择企业会员,我们对企业会员产品有严格审核。 公司名称: PLATTE 推荐 投诉 收藏 联系电话: 308 537 3900 电子邮件: info@plattevalleyscientific.com 国籍: 美国 产品介绍: CB指数: 30 网址: www.plattevalleyscientific.com 相关信息: 全球销售网络 产品目录(3735...
阿拉丁试剂为您精选了相关的许多ML-167,Cdc2样激酶4抑制剂,[5-[4-[(5-甲基呋喃-2-基)甲基氨基]喹唑啉-6-基]呋喃-2-基]甲醇 | NCGC00188654-04 | [5-(4-{[(5-METHYLFURAN-2-YL)METHYL]AMINO}QUINAZOLIN-6-YL)FURAN-2-YL]METHANOL | BDBM50342913 | AC-35934 | s7509 | [5-[4-
PECULIAR SHARPLESS KINETIC RESOLUTION OF 2-FURYLMETHANOL AND ITS APPLICATION TO THE SYNTHESIS OF (+)-ASPERLINOptically-active 2-furylcarbinolsReagent(+)-acetylphomalactoneEpoxidationA peculiar kinetic resolution of E-1-(2-furyl)-2-buten-1-ol (1), which produced two products, pyranone (2) and...
The Paternò–Büchi reaction between 2-furylmethanol derivatives and aliphatic aldehydes and ketones induced by irradiation through Vycor at 8°C shows high regioselectivity but no stereoselectivity. This behaviour can be rationalised by assuming that this type of compound reacts through both singlet ...