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Merck

160954

Sigma-Aldrich

对硝基苯磺酸甲酯

99%

别名:

Methyl nosylate, Methyl p-nitrobenzenesulfonate, Methyl p-nitrotosylate

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About This Item

线性分子式:
O2NC6H4SO3CH3
CAS号:
分子量:
217.20
Beilstein:
2277327
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

99%

形狀

solid

mp

89-92 °C (lit.)

溶解度

acetone: soluble 5%, clear, faintly yellow to greenish-yellow

官能基

nitro
sulfonic acid

SMILES 字串

COS(=O)(=O)c1ccc(cc1)[N+]([O-])=O

InChI

1S/C7H7NO5S/c1-13-14(11,12)7-4-2-6(3-5-7)8(9)10/h2-5H,1H3

InChI 密鑰

RMNJNEUWTBBZPT-UHFFFAOYSA-N

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一般說明

Reaction between methyl 4-nitrobenzenesulfonate and bromide ions has been studied in mixed single-chain-gemini micellar solutions. Kinetics of SN2 reactions of methyl 4-nitrobenzenesulfonate with ammonia, primary amines, secondary amines, tertiary amines and anionic nucleophiles has been studied.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Skin Irrit. 2

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)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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S Ishii et al.
Protein science : a publication of the Protein Society, 7(8), 1802-1810 (1999-03-19)
Aromatic L-amino acid decarboxylase (AADC) catalytic mechanism has been proposed to proceed through two consecutive intermediates (i.e., Michaelis complex and the external aldimine). Limited proteolysis of AADC that preferentially digested at the C-terminal side of Arg334 was slightly retarded in
O Paquatte et al.
Photochemistry and photobiology, 50(6), 817-825 (1989-12-01)
Vibrio harveyi luciferase, an alpha beta dimer, was effectively inactivated by treatment with the methylation agent methyl p-nitrobenzene sulfonate. However, inactivation of luciferase in the presence of excess amounts of this reagent did not follow pseudo-first-order kinetics. After taking the
T Kohzuma et al.
Journal of biochemistry, 106(6), 1054-1058 (1989-12-01)
When Trimeresurus flavoviridis phospholipase A2 was reacted with methyl p-nitrobenzenesulfonate, its activity decreased following first-order kinetics. The pH dependence of the rate constants of inactivation showed that His-48 with an apparent pKa of 6.5 controls the reaction. In the pH
Cysteine modification of metallothionein.
P E Hunziker
Methods in enzymology, 205, 399-400 (1991-01-01)
J P Marcus et al.
Archives of biochemistry and biophysics, 316(1), 413-420 (1995-01-10)
Incubation of L-threonine dehydrogenase from Escherichia coli with methyl p-nitrobenzenesulfonate results in a time- and concentration-dependent loss of enzymatic activity. As the concentration of the methylating agent is increased, the rate of inactivation reaches a limiting value of 0.01 min-1

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