139076
1-乙酰基-5-溴-4-氯吲哚-3-乙酸酯
98%
别名:
5-溴-4-氯-3-吲哚基-1,3-二乙酸酯
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关于此项目
经验公式（希尔记法）:
C12H9BrClNO3
化学文摘社编号:
分子量:
330.56
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
221-200-6
Beilstein/REAXYS Number:
270885
MDL number:
Assay:
98%
InChI key
DSHQTSIXXYZXGR-UHFFFAOYSA-N
InChI
1S/C12H9BrClNO3/c1-6(16)15-5-10(18-7(2)17)11-9(15)4-3-8(13)12(11)14/h3-5H,1-2H3
SMILES string
CC(=O)Oc1cn(C(C)=O)c2ccc(Br)c(Cl)c12
assay
98%
mp
165-168 °C (lit.)
solubility
chloroform: soluble 50 mg/mL, clear, pale yellow to yellow
storage temp.
2-8°C
Application
5-Bromo-4-chloroindoxyl 1,3-diacetate was used as starting reagent in the synthesis of 5,5′-dibromo-4,4′-dichloroindigo.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Faten Arab-Jaziri et al.
New biotechnology, 30(5), 536-544 (2013-05-01)
Directed evolution was applied to the α-l-arabinofuranosidase from Thermobacillus xylanilyticus to confer better transglycosylation ability, particularly for the synthesis of benzyl α-l-arabinofuranosyl-(1,2)-α-d-xylopyranoside, starting from p-nitrophenyl α-l-arabinofuranoside (donor) and benzyl α-d-xylopyranoside (acceptor). The aim was to obtain mutants displaying both lower
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