432040
苄氧乙酸
95%
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关于此项目
线性分子式:
C6H5CH2OCH2CO2H
化学文摘社编号:
分子量:
166.17
UNSPSC Code:
12352100
MDL number:
NACRES:
NA.22
PubChem Substance ID:
产品名称
苄氧乙酸, 95%
InChI
1S/C9H10O3/c10-9(11)7-12-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)
SMILES string
OC(=O)COCc1ccccc1
InChI key
GRZHHTYDZVRPIC-UHFFFAOYSA-N
assay
95%
form
liquid
refractive index
n20/D 1.526 (lit.)
bp
137-139 °C/0.6 mmHg (lit.)
density
1.162 g/mL at 25 °C (lit.)
functional group
carboxylic acid
ether
phenyl
Quality Level
Other Notes
可能含氯乙酸
Application
Benzyloxyacetic acid may be used for the following syntheses:
- mixed benzyloxyacetic pivalic anhydride
- chiral glycolates, 1,2:4,5-di-O-isopropylidene-β-D-fructopyranos-3-yl benzyloxyacetate, via esterification
- tetraaqua(1,10-phenanthroline-[κ]2N,N′)magnesium(II) bis[(2,4-dichlorophenyl)acetate]
- as ligand in the preparation of diaquabis(benzyloxyacetato)copper(II) complex
General description
In vitro activities of phenoxy and benzyloxyacetic acid derivatives as antisickling agents has been investigated by the application of quantitative structure activity relationship (QSAR) of Hansch-type.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Xiao-Min Hao et al.
Acta crystallographica. Section E, Structure reports online, 64(Pt 8), m1052-m1052 (2008-01-01)
In the mononuclear title complex, [Mg(C(12)H(8)N(2))(H(2)O)(4)](C(8)H(5)Cl(2)O(2))(2), each Mg(II) ion is hexa-coordinated by two N atoms from a 1,10-phenanthroline ligand [Mg-N = 2.233 (2) Å] and four water mol-ecules [Mg-OW = 2.033 (2) and 2.043 (1) Å] in a distorted octa-hedral geometry. A twofold rotation axis
A highly effective asymmetric synthesis of a-hydroxy acids by alkylation of chiral n-(benzyloxyacetyl)-trans-2, 5-bis (methoxymethoxymethyl) pyrrolidine.
Enomoto M, et al.
Tetrahedron Letters, 26(10), 1343-1344 (1985)
An inexpensive carbohydrate derivative used as a chiral auxiliary in the synthesis of a-hydroxy carboxylic acids.
Yu H, et al.
Tetrahedron, 58(38), 7663-7669 (2002)
M A Mahran
Bollettino chimico farmaceutico, 139(2), 73-80 (2000-08-02)
Quantitative structure activity relationship of Hansch-type has been applied to develop correlation between the calculated physicochemical properties and the in vitro activities of phenoxy and benzyloxyacetic acid derivatives as antisickling agents. The antisickling effect of these compounds was first reported
Diaquabis (benzyloxyacetato) copper (II).
Sun S-L, et al.
Acta Crystallographica Section E, Structure Reports Online, 64(5), 1052-1052 (2008)
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