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339598

Sigma-Aldrich

4-氨基-3-羟基苯甲酸

97%

别名:

3-Hydroxy-4-aminobenzoic acid, 3-Hydroxy-PABA

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About This Item

线性分子式:
H2NC6H3(OH)CO2H
CAS号:
2374-03-0
分子量:
153.14
Beilstein:
509859
MDL编号:
MFCD00017094
UNSPSC代码:
12352106
eCl@ss:
32160406
PubChem化学物质编号:
24860651
NACRES:
NA.22

质量水平

100

方案

97%

表单

solid

反应适用性

reaction type: solution phase peptide synthesis

mp

211-215 °C (lit.)

应用

peptide synthesis

SMILES字符串

Nc1ccc(cc1O)C(O)=O

InChI

1S/C7H7NO3/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3,9H,8H2,(H,10,11)

InChI key

NFPYJDZQOKCYIE-UHFFFAOYSA-N

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相关类别

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险分类

Acute Tox. 4 Oral - 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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000332065
0000362587
0000347382
0000286401
0000286402

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Falicia Goh et al.
Microbial cell factories, 19(1), 71-71 (2020-03-21)
Notonesomycin A is a 32-membered bioactive glycosylated macrolactone known to be produced by Streptomyces aminophilus subsp. notonesogenes 647-AV1 and S. aminophilus DSM 40186. In a high throughput antifungal screening campaign, we identified an alternative notonesomycin A producing strain, Streptomyces sp.
Kerim Babaoglu et al.
Nature chemical biology, 2(12), 720-723 (2006-10-31)
Fragment-based screens test multiple low-molecular weight molecules for binding to a target. Fragments often bind with low affinities but typically have better ligand efficiencies (DeltaG(bind)/heavy atom count) than traditional screening hits. This efficiency, combined with accompanying atomic-resolution structures, has made
Jinkyu Park et al.
Journal of hazardous materials, 371, 243-252 (2019-03-11)
Carboxylate-functionalized organic nanocrystals (ONCs) derived from perylene diimide or naphthalene diimide were synthesized and carefully characterized as novel high-capacity uranium (U(VI)) sorbents. Adsorption studies using uranyl ions demonstrated that the carboxyl and hydroxyl groups on the surface of the ONCs
Chao-Bin Xue et al.
Bioorganic & medicinal chemistry, 15(5), 2006-2015 (2007-01-30)
Phenoloxidase (PO), also known as tyrosinase, is a key enzyme in insect development, responsible for catalyzing the hydroxylation of tyrosine into o-diphenols and the oxidation of o-diphenols into o-quinones. Inhibition of PO may provide a basis for novel environmentally friendly

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