推薦產品
化驗
97%
形狀
liquid
折射率
n20/D 1.527 (lit.)
bp
136 °C/14 mmHg (lit.)
密度
1.171 g/mL at 25 °C (lit.)
SMILES 字串
OCC(=O)OCc1ccccc1
InChI
1S/C9H10O3/c10-6-9(11)12-7-8-4-2-1-3-5-8/h1-5,10H,6-7H2
InChI 密鑰
VPYJBEIOKFRWQZ-UHFFFAOYSA-N
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一般說明
乙醇酸苄酯是乙醇酸的一种苄基酯。
應用
乙醇酸苄酯可被用于合成[2-(2′-苄氧基-2′-氧乙基)-5-乙酰氨基-4,7,8,9-四-O-乙酰基-3,5-二脱氧-α-和-β-D-甘油-D-半乳糖-2-壬基吡喃糖苷]甲酯。它可用于制备单糖构建单元。它也可用于合成以下具有乙醇酸侧酯或以乳酸作为侧基的新型聚合磷腈:
- 聚[双(乙基乙二醇基)磷腈]
- 聚[双(乙基乳酸)磷腈]
- 聚[双(苄基乙二醇基)磷腈]
- 聚[双(苄基内氨基)磷腈]
儲存類別代碼
10 - Combustible liquids
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
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。
Chemistry (Weinheim an der Bergstrasse, Germany), 9(5), 1085-1095 (2003-02-22)
A facile synthesis of the sialic acid oligomers alpha-(2-->5)Neu5Gc (1) is presented. Monosaccharides 2-4 with suitable functionality were used as the building blocks. After selective removal of the paired carboxyl and amine protecting groups, the fully protected oligomers were assembled
The Journal of organic chemistry, 67(4), 1376-1379 (2002-02-16)
The preparation of a disaccharide 2, Neu5Ac-alpha-(2-->5)Neu5Gc having a alpha-benzyl protecting group at the reducing end, by the coupling of the easily accessible building units 4 and 5 is described. Subsequent deprotection of the coupling adduct led to the isolation
Synthesis of poly (orgnaophosphazenes) with glycolic acid ester and lactic acid ester side groups: Prototypes for new bioerodible polymers.
Macromolecules, 27(1), 1-4 (1994)
我們的科學家團隊在所有研究領域都有豐富的經驗,包括生命科學、材料科學、化學合成、色譜、分析等.
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