추천 제품
분석
95%
형태
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.)
SMILES string
OC(=O)COCc1ccccc1
InChI
1S/C9H10O3/c10-9(11)7-12-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)
InChI key
GRZHHTYDZVRPIC-UHFFFAOYSA-N
일반 설명
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.
애플리케이션
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
기타 정보
may contain chloroacetic acid
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
235.4 °F - closed cup
Flash Point (°C)
113 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
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
An inexpensive carbohydrate derivative used as a chiral auxiliary in the synthesis of a-hydroxy carboxylic acids.
Tetrahedron, 58(38), 7663-7669 (2002)
Diaquabis (benzyloxyacetato) copper (II).
Acta Crystallographica Section E, Structure Reports Online, 64(5), 1052-1052 (2008)
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
A highly effective asymmetric synthesis of a-hydroxy acids by alkylation of chiral n-(benzyloxyacetyl)-trans-2, 5-bis (methoxymethoxymethyl) pyrrolidine.
Tetrahedron Letters, 26(10), 1343-1344 (1985)
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