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Merck

139076

Sigma-Aldrich

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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About This Item

经验公式(希尔记法):
C12H9BrClNO3
CAS号:
分子量:
330.56
Beilstein:
270885
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

98%

mp

165-168 °C (lit.)

溶解度

chloroform: soluble 50 mg/mL, clear, pale yellow to yellow

儲存溫度

2-8°C

SMILES 字串

CC(=O)Oc1cn(C(C)=O)c2ccc(Br)c(Cl)c12

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

InChI 密鑰

DSHQTSIXXYZXGR-UHFFFAOYSA-N

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應用

5-Bromo-4-chloroindoxyl 1,3-diacetate was used as starting reagent in the synthesis of 5,5′-dibromo-4,4′-dichloroindigo.

儲存類別代碼

11 - Combustible Solids

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, type N95 (US)


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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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