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516422

4-甲氧基-3-硝基苯甲醛

Name: 4-甲氧基-3-硝基苯甲醛
Brand: ALDRICH

97%

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关于此项目

线性分子式:

CH₃OC₆H₃(NO₂)CHO

化学文摘社编号:

31680-08-7

分子量:

181.15

NACRES:

NA.22

PubChem Substance ID:

24873889

UNSPSC Code:

12352100

MDL number:

MFCD00126498

Assay:

97%

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属性

assay

97%

mp

97-100 °C (lit.)

functional group

aldehyde, nitro

SMILES string

COc1ccc(C=O)cc1[N+]([O-])=O

InChI

1S/C8H7NO4/c1-13-8-3-2-6(5-10)4-7(8)9(11)12/h2-5H,1H3

InChI key

YTCRQCGRYCKYNO-UHFFFAOYSA-N

说明

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)

历史批次信息供参考:

分析证书(COA)

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Supported bilayer lipid membrane arrays on photopatterned self-assembled monolayers.

Xiaojun Han et al.

Chemistry (Weinheim an der Bergstrasse, Germany), 13(28), 7957-7964 (2007-07-06)

This work demonstrates the use of photocleavable cholesterol derivatives to create supported bilayer lipid membrane arrays on silica. The photocleavable cholesteryl tether is attached to the surface by using the reaction of an amine-functionalized self-assembled monolayer (SAM) and the N-hydroxysuccinimide-based

Tele nucleophilic aromatic substitutions in 1-nitro-3-and 1, 3-dinitro-5-trichloromethylbenzene, and 3-trichloromethylbenzonitrile. A new synthesis of the 1, 4-benzothiazine-3 (4H)-one ring system from 3-nitrobenzoic acid.

Giannopoulos T, et al.

Tetrahedron, 56(3), 447-453 (2000)

Synthesis, cytotoxic activity and docking studies of new 4-aza-podophyllotoxin derivatives.

Hatti I, et al.

Medicinal Chemistry Research, 24(8), 3305-3313 (2015)

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全球贸易项目编号

货号	GTIN
516422-5G	04061831830095