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About This Item
线性分子式:
Cl2C6H3CH2OH
CAS号:
分子量:
177.03
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
推荐产品
化驗
98%
形狀
solid
mp
79-82 °C (lit.)
SMILES 字串
OCc1cc(Cl)cc(Cl)c1
InChI
1S/C7H6Cl2O/c8-6-1-5(4-10)2-7(9)3-6/h1-3,10H,4H2
InChI 密鑰
VSNNLLQKDRCKCB-UHFFFAOYSA-N
應用
3,5-Dichlorobenzyl alcohol was used in the preparation of 3,5-dichlorophenylacetonitrile via reaction with boiling SOCl2, followed by reaction with NaCN. It was also used in the synthesis of tert-butyl 2-cyano-3-(3,5-dichlorophenyl)-propanoate via Iridium-catalysed alkylation of tert-butyl cyanoacetate.
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
Iridium catalysed alkylation of tert-butyl cyanoacetate with alcohols under solvent free conditions.
Grigg R, et al.
Tetrahedron, 65(4), 849-854 (2009)
Esben R Sørensen et al.
Archiv der Pharmazie, 338(7), 299-304 (2005-07-05)
The HIV-1 inhibitors described in this paper is closely related to 6-(3,5-dimethylbenzyl)-1-(ethoxy methyl)-5-isopropyluracil (GCA-186) an anti-HIV-1 drug that is highly active against both wild type and mutated HIV-1 strains. The two methyl groups on the 6-benzyl moiety have been shown
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