登录 查看组织和合同定价。
选择尺寸
关于此项目
线性分子式:
CH3OCH2COCl
化学文摘社编号:
分子量:
108.52
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
254-169-2
Beilstein/REAXYS Number:
1740244
MDL number:
Assay:
97%
Form:
liquid
InChI key
JJKWHOSQTYYFAE-UHFFFAOYSA-N
InChI
1S/C3H5ClO2/c1-6-2-3(4)5/h2H2,1H3
SMILES string
COCC(Cl)=O
assay
97%
form
liquid
refractive index
n20/D 1.419 (lit.)
bp
112-113 °C (lit.)
density
1.187 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
正在寻找类似产品? 访问 产品对比指南
Application
甲氧基乙酰氯可用于以下物质的甲氧基乙酰化反应:
也可用于合成 β——内酰胺,通过与亚胺反应 ,并在金属-有机骨架 (MOF) 的后合成修饰中,MIL-101,合成了一种催化剂,用于 CO 2 与环氧丙烷的环加成反应。
- 双叶脲 A,合成 8-甲氧基乙酰氧基双叶脲 A。
- 取代和未取代苯甲酰胺合成 N -(2-甲氧基乙酰基)-苯甲酰胺。
也可用于合成 β——内酰胺,通过与亚胺反应 ,并在金属-有机骨架 (MOF) 的后合成修饰中,MIL-101,合成了一种催化剂,用于 CO 2 与环氧丙烷的环加成反应。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
82.4 °F
flash_point_c
28 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Radu A Gropeanu et al.
PloS one, 7(9), e43657-e43657 (2012-09-13)
Three different variants of photoactivatable caged paclitaxel (PTX) have been synthesized and their bioactivity was characterized in in vitro assays and in living cells. The caged PTXs contain the photoremovable chromophore 4,5-dimethoxy-2-nitrobenzyloxycarbonyl (Nvoc) attached to position C7, C2' and to
An investigation towards the diastereoselective synthesis of 3-acetoxy/methoxy/phthalimido-β-lactams using chiral imines.
Bhalla A, et al.
Tetrahedron Asymmetry, 28(2), 307-316 (2017)
Bioactive dihydro-?-agarofuran sesquiterpenoids from the Australian rainforest plant Maytenus bilocularis.
Wibowo M, et al.
Journal of Natural Products, 79(5), 1445-1453 (2016)
Functionalized MIL-101 with imidazolium-based ionic liquids for the cycloaddition of CO2 and epoxides under mild condition.
Liu D, et al.
Applied Surface Science, 428(45), 218-225 (2018)
A telescopic one-pot synthesis of ?-lactam rings using amines as a convenient source of imines.
Rajamaki SHM, et al.
Royal Society of Chemistry Advances, 6(45), 38553-38557 (2016)
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持

