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Merck
CN

C105805

Sigma-Aldrich

环己甲醇

ReagentPlus®, ≥99%

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别名:
(羟甲基)环己烷, NSC 5288, 六氢苯甲醇, 环己基甲醇
线性分子式:
C6H11CH2OH
CAS号:
分子量:
114.19
Beilstein:
773712
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

产品线

ReagentPlus®

检测方案

≥99%

形式

liquid

折射率

n20/D 1.465 (lit.)

bp

181 °C (lit.)

密度

0.928 g/mL at 25 °C (lit.)

SMILES字符串

OCC1CCCCC1

InChI

1S/C7H14O/c8-6-7-4-2-1-3-5-7/h7-8H,1-6H2

InChI key

VSSAZBXXNIABDN-UHFFFAOYSA-N

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应用

环己甲醇(环己基甲醇)可作为起始材料,使用二氧化钛纳米颗粒作为催化剂,通过光催化氧化 (PCO) 合成环己甲醛、环己甲酸、环己酮和1,4-环己二酮。

法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

WGK

WGK 1

闪点(°F)

170.6 °F

闪点(°C)

77 °C

个人防护装备

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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Nanoparticles TiO2-photocatalyzed oxidation of selected cyclohexyl alcohols.
Mohamed OS, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 200(2-3), 209-215 (2008)
Yasunori Okada et al.
Organic letters, 9(8), 1573-1576 (2007-03-16)
[reaction: see text] Ethyl 1-thio-2,3,4,6-tetrakis-O-triisopropylsilyl-beta-d-glucopyranoside, ethyl 6-O-benzyl-1-thio-2,3,4-tris-O-triisopropylsilyl-beta-d-glucopyranoside, and ethyl 6-O-pivaloyl-1-thio-2,3,4-tris-O-triisopropylsilyl-beta-d-glucopyranoside induced highly beta-selective O-glucosidations. Among them, the 6-O-pivaloylated substrate provided the best selectivity up to alpha/beta = 3:97 with cyclohexylmethanol, and the substrate was used for glucosidations with secondary and
Rabea Schlüter et al.
Applied microbiology and biotechnology, 103(10), 4137-4151 (2019-04-04)
The cycloalkanes, comprising up to 45% of the hydrocarbon fraction, occur in crude oil or refined oil products (e.g., gasoline) mainly as alkylated cyclohexane derivatives and have been increasingly found in environmental samples of soil and water. Furthermore, short-chain alkylated

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