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193836

Sigma-Aldrich

3-甲氧基-4-硝基苯甲醇

99%

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1 MG
¥1,790.01

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预计发货时间2025年3月24日详情


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1 MG
¥1,790.01

About This Item

线性分子式:
CH3OC6H3(NO2)CH2OH
CAS号:
分子量:
183.16
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

¥1,790.01


预计发货时间2025年3月24日详情


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方案

99%

表单

solid

mp

95-97 °C (lit.)

官能团

hydroxyl
nitro

SMILES字符串

COc1cc(CO)ccc1[N+]([O-])=O

InChI

1S/C8H9NO4/c1-13-8-4-6(5-10)2-3-7(8)9(11)12/h2-4,10H,5H2,1H3

InChI key

AADYWCBPJZAJNU-UHFFFAOYSA-N

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此商品
187291154113187895
3-溴苄醇 99%

187895

3-溴苄醇

mp

95-97 °C (lit.)

mp

69-73 °C (lit.)

mp

-

mp

-

form

solid

form

solid

form

liquid

form

liquid

应用

3-Methoxy-4-nitrobenzyl alcohol was used in the synthesis of:
  • 3-methoxy-4-nitrobenzyl azide[1]
  • new aryl azides, (Z)-1-(3′-azido-4′-methoxyphenyl)-2-(3″,4″,5″-trimethoxyphenyl)ethane and (Z)-1-(4′-azido-3′-methoxyphenyl)-2-(3″,4″,5″-trimethoxyphenyl)ethane, potentially useful photoaffinity labeling reagents for tubulin[2]
  • 3-methoxy-4-nitrobenzaldehyde via oxidation[3]
  • 4-[3-(2-methylphenyl)ureido]-3-methoxybenzylchloride, required for syntheses of trifluoromethyl-substituted hydantoins[4]

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

新产品

  • 历史批次信息供参考:

    分析证书(COA)

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    K G Pinney et al.
    Bioorganic & medicinal chemistry, 8(10), 2417-2425 (2000-11-01)
    Two new aryl azides, (Z)-1-(3'-azido-4'-methoxyphenyl)-2-(3",4",5"-trimethoxyphenyl)ethene 9 and (Z)-1-(4'-azido-3'-methoxyphenyl)-2-(3",4",5"-trimethoxyphenyl)ethene 5, modeled after the potent antitumor, antimitotic agent combretastatin A-4 (CA-4), have been prepared by chemical synthesis as potentially useful photoaffinity labeling reagents for the colchicine site on beta-tubulin. Aryl azide 9
    Jeewoo Lee et al.
    Journal of medicinal chemistry, 46(14), 3116-3126 (2003-06-27)
    Isosteric replacement of the phenolic hydroxyl group in potent vanilloid receptor (VR1) agonists with the alkylsulfonamido group provides a series of compounds which are effective antagonists to the action of the capsaicin on rat VR1 heterologously expressed in Chinese hamster
    Trifluoromethyl-substituted hydantoins, versatile building blocks for rational drug design.
    Wehner V, et al.
    Tetrahedron, 60(19), 4295-4302 (2004)
    Can we predict reactivity for aromatic nucleophilic substitution with [18F] fluoride ion?
    Rengan R, et al.
    Journal of Labelled Compounds & Radiopharmaceuticals, 33(7), 563-572 (1993)

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