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189286

4-硝基苯甲酰胺

98%

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关于此项目

线性分子式:
O2NC6H4CONH2
化学文摘社编号:
619-80-7
分子量:
166.13
NACRES:
NA.22
PubChem Substance ID:
24851375
UNSPSC Code:
12352100
EC Number:
210-613-7
MDL number:
MFCD00007994
Assay:
98%
Form:
solid
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Quality Level

100

assay

98%

form

solid

mp

199-201 °C (lit.)

functional group

amide, nitro

SMILES string

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

InChI

1S/C7H6N2O3/c8-7(10)5-1-3-6(4-2-5)9(11)12/h1-4H,(H2,8,10)

InChI key

ZESWUEBPRPGMTP-UHFFFAOYSA-N

General description

Negative quasimolecular ions of 4-nitrobenzamide has been investigated by electrospray ionization mass spectrometry.

Application

4-Nitrobenzamide was used in the preparation of 4-nitrobenziminosulfurane.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCK4333
95597KJ
S39550
03909EW
13330PZ

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F C Chiu et al.
Journal of the American Society for Mass Spectrometry, 11(12), 1061-1064 (2000-01-11)
Negative quasimolecular ions of aromatic carboxylic acid amides have been observed unexpectedly under electrospray ionization conditions. Hypothetically, deprotonation of either carboxamide or carboximidic acid tautomers can produce anions with equivalent resonance structures, the stability of which is affected by conjugated
Preparation of nitriles from primary amides under Swern oxidation conditions.
Nakajima N and Ubukata M.
Tetrahedron Letters, 38(12), 2099-2102 (1997)

全球贸易项目编号

货号GTIN
189286-25G04061831819014
189286-5G04061838759122