C105805
环己甲醇
ReagentPlus®, ≥99%
别名:
(羟甲基)环己烷, NSC 5288, 六氢苯甲醇, 环己基甲醇
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线性分子式:
C6H11CH2OH
化学文摘社编号:
分子量:
114.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-857-8
Beilstein/REAXYS Number:
773712
MDL number:
Assay:
≥99%
Form:
liquid
产品名称
环己甲醇, ReagentPlus®, ≥99%
InChI key
VSSAZBXXNIABDN-UHFFFAOYSA-N
InChI
1S/C7H14O/c8-6-7-4-2-1-3-5-7/h7-8H,1-6H2
SMILES string
OCC1CCCCC1
product line
ReagentPlus®
assay
≥99%
form
liquid
refractive index
n20/D 1.465 (lit.)
bp
181 °C (lit.)
density
0.928 g/mL at 25 °C (lit.)
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Application
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。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
170.6 °F - closed cup
flash_point_c
77 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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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