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Merck
CN

21873

对甲酰基苯甲酸

purum, ≥95.0% (T)

别名:

4-羧基苯甲醛, 对醛基苯甲酸, 苯甲醛对羧酸

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线性分子式:
HO2CC6H4CHO
化学文摘社编号:
619-66-9
分子量:
150.13
EC Number:
210-607-4
UNSPSC Code:
12352100
PubChem Substance ID:
24853080
Beilstein/REAXYS Number:
471734
MDL number:
MFCD00006951

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grade

purum

assay

≥95.0% (T)

mp

247 °C (lit.)

SMILES string

[H]C(=O)c1ccc(cc1)C(O)=O

InChI

1S/C8H6O3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5H,(H,10,11)

InChI key

GOUHYARYYWKXHS-UHFFFAOYSA-N

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存储类别

13 - Non 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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Yves Meyer et al.
Organic & biomolecular chemistry, 8(8), 1777-1780 (2010-05-08)
This study focuses on the disassembly-behavior of self-immolative pro-fluorescent linkers under physiological conditions and through an enzyme-initiated domino reaction. The targeted linkers are based on para-aminobenzylalcohol (PABA) or hemithioaminal derivatives of para-carboxybenzaldehyde or glyoxilic acid. We found that a fine
C M Ryle et al.
The Biochemical journal, 197(3), 715-720 (1981-09-01)
The distribution of the two principal isoenzymes of aldehyde reductase (EC 1.1.1.2) has been studied in ox brain. The more active of these, which has been termed the high-Km enzyme, has been shown to be located in the cytosol and
A Magnien et al.
European journal of biochemistry, 131(2), 375-381 (1983-03-15)
Initial-rate measurements were made of the reduction of pyridine-3-aldehyde and p-carboxybenzaldehyde by NADPH catalyzed by pig liver aldehyde reductase I. The initial velocity analysis and product inhibition data suggest that aldehyde reductase I obeys a compulsory-order mechanism with pyridine-3-aldehyde as
Da Huang et al.
Biomaterials, 52, 417-425 (2015-03-31)
Bone tuberculosis (TB) is one of the most common extrapulmonary TB. Effective integration of chemotherapy and bone regeneration is an optimal solution for bone TB therapy. Herein, we produce a composite scaffold drug delivery system fabricated with an isoniazid conjugated

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