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Merck
모든 사진(1)

주요 문서

58279

Sigma-Aldrich

Isatoic anhydride

technical, ≥94% (HPLC)

동의어(들):

3,1-Benzoxazine-2,4(1H)-dione, Anthranilic acid N-carboxylic acid anhydride

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About This Item

실험식(Hill 표기법):
C8H5NO3
CAS Number:
Molecular Weight:
163.13
Beilstein:
136786
EC Number:
MDL number:
UNSPSC 코드:
12162002
PubChem Substance ID:

vapor density

5.6 (vs air)

grade

technical

분석

≥94% (HPLC)

mp

233 °C (dec.) (lit.)

SMILES string

O=C1Nc2ccccc2C(=O)O1

InChI

1S/C8H5NO3/c10-7-5-3-1-2-4-6(5)9-8(11)12-7/h1-4H,(H,9,11)

InChI key

TXJUTRJFNRYTHH-UHFFFAOYSA-N

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기타 정보

Review; Reagent for 2-aminobenzoylations

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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

M.C. Venuti
Synthesis, 266-266 (1982)
G.M. Coppola
Synthesis, 505-505 (1980)
M G Page
The Biochemical journal, 295 ( Pt 1), 295-304 (1993-10-01)
Class C beta-lactamases from Pseudomonas aeruginosa and several species of the Enterobacteriaceae have been observed to undergo a rapid burst in hydrolysis of beta-lactam antibiotics before relaxation to a steady-state rate of hydrolysis. The amplitude of the burst corresponds to
Christine Hiu-Tung Chen et al.
Molecular diversity, 9(4), 353-359 (2005-11-29)
Reactions using fluorous reagents and scavengers are compared side-by-side with their solid-supported counterparts. Fluorous triphenylphosphine is used in the bromination reaction of alcohols, fluorous thiol is used as an electrophile scavenger for alpha-bromoketones, fluorous isatoic anhydride is used as a
J E Churchich
Analytical biochemistry, 213(2), 229-233 (1993-09-01)
Isatoic anhydride reacts with nucleophile groups of proteins to yield o-aminobenzoyl protein conjugates. The fluorescence emitted by the chromophore decays in a multiexponential manner with average fluorescence lifetimes ranging from 9.9 to 10.7 ns. The steady emission anisotropy, measured upon

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