189081
顺-1,2-环己二甲醇
97%
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关于此项目
线性分子式:
C6H10(CH2OH)2
化学文摘社编号:
分子量:
144.21
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
239-843-6
MDL number:
Assay:
97%
Form:
solid
InChI key
XDODWINGEHBYRT-OCAPTIKFSA-N
InChI
1S/C8H16O2/c9-5-7-3-1-2-4-8(7)6-10/h7-10H,1-6H2/t7-,8+
SMILES string
OC[C@@H]1CCCC[C@@H]1CO
assay
97%
form
solid
mp
43-45 °C (lit.)
General description
Enantioselective oxidation of cis-1,2-cyclohexanedimethanol using 4-acetylamino-2,2,7-trimethyl-10-isopropyl-1-azaspiro[5.5]undecane N-oxyl as a chiral nitroxyl radical via non-electrochemical method has been reported.
Application
cis-1,2-Cyclohexanedimethanol was used in the synthesis of 9-{[(Z)-2(hydroxymethyl)cyclohexyl]methyl}guanine (L-653,180).
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Sanjiv O Tomer et al.
Organic & biomolecular chemistry, 15(42), 8990-8997 (2017-10-19)
We have experimentally demonstrated that by 'locking' the molecular conformation through the introduction of a double or triple bond in the center of a symmetric diol, enzymatic monoesterification can be achieved selectively. The enzyme Candida antarctica lipase B, generally used
N Bourne et al.
Antimicrobial agents and chemotherapy, 36(9), 2020-2024 (1992-09-01)
Herpes simplex virus (HSV)-coded thymidine kinase (TK) is important in efficient reactivation of latent infection. These studies were designed to investigate whether treatment of latently infected animals with a TK inhibitor altered the natural history of recurrent HSV disease. 9-([(Z)-2-(hydroxymethyl)cyclohexyl]methyl)
Enantioselective Oxidation of Secondary Alcohols Using a Chiral Nitroxyl (N-Oxoammonium salt) Catalyst.
Rychnovsky SD, et al.
The Journal of Organic Chemistry, 61(4), 1194-1195 (1996)
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