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Merck
CN

140392

4-羟基-3,5-二甲基苯甲醛

95%

别名:

3,5-二甲基-4-羟基苯甲醛

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关于此项目

线性分子式:
HOC6H2(CH3)2CHO
化学文摘社编号:
分子量:
150.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-774-5
Beilstein/REAXYS Number:
1908717
MDL number:
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产品名称

4-羟基-3,5-二甲基苯甲醛, 95%

InChI key

UYGBSRJODQHNLQ-UHFFFAOYSA-N

InChI

1S/C9H10O2/c1-6-3-8(5-10)4-7(2)9(6)11/h3-5,11H,1-2H3

SMILES string

[H]C(=O)c1cc(C)c(O)c(C)c1

assay

95%

mp

112-114 °C (lit.)

functional group

aldehyde

Quality Level

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Application

4-Hydroxy-3,5-dimethylbenzaldehydewas used as reagent during the phase transfer catalyzed polymerization of 4-hydroxy-3,5-dimethylbenzyl alcohol. It was used as starting reagent during the synthesis of 2,4,6-trimethylphenol.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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D J Abraham et al.
Biochemistry, 34(46), 15006-15020 (1995-11-21)
Monoaldehyde allosteric effectors of hemoglobin were designed, using molecular modeling software (GRID), to form a Schiff base adduct with the Val 1 alpha N-terminal nitrogens and interact via a salt bridge with Arg 141 alpha of the opposite subunit. The
A facile synthesis of 4-alkoxymethylphenols by a copper (II)-acetoxime catalyst/O2 system.
Shimizu M, et al.
Tetrahedron Letters, 32(18), 2053-2056 (1991)
Phase transfer catalyzed polymerization of 4-hydroxy-3, 5-dimethylbenzyl alcohol and copolymerization of 4-bromo-2, 6-dimethylphenol with 4-hydroxy-3, 5-dimethylbenzyl alcohol.
Wang JH and Percec V.
Polym. Bull., 25(1), 25-32 (1991)
P R Ortiz de Montellano et al.
The Journal of biological chemistry, 262(24), 11641-11646 (1987-08-25)
Chloroperoxidase and H2O2 oxidize styrene to styrene oxide and phenylacetaldehyde but not benzaldehyde. The epoxide oxygen is shown by studies with H2(18)O2 to derive quantitatively from the peroxide. The epoxidation of trans-[1-2H]styrene by chloroperoxidase proceeds without detectable loss of stereochemistry

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