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Merck
CN

339598

4-氨基-3-羟基苯甲酸

97%

别名:

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

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关于此项目

线性分子式:
H2NC6H3(OH)CO2H
化学文摘社编号:
分子量:
153.14
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352106
MDL number:
Beilstein/REAXYS Number:
509859
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产品名称

4-氨基-3-羟基苯甲酸, 97%

InChI

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

SMILES string

Nc1ccc(cc1O)C(O)=O

InChI key

NFPYJDZQOKCYIE-UHFFFAOYSA-N

assay

97%

form

solid

reaction suitability

reaction type: solution phase peptide synthesis

mp

211-215 °C (lit.)

application(s)

peptide synthesis

Quality Level

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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

Lot/Batch Number

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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
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.
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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