554154
4- 叔 -丁基-2,6-二甲酰苯酚
96%
别名:
5-(1,1-二甲基乙基)-2-羟基-1,3-苯二甲醛
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关于此项目
线性分子式:
(CH3)3CC6H2(CHO)2OH
化学文摘社编号:
分子量:
206.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
96%
InChI
1S/C12H14O3/c1-12(2,3)10-4-8(6-13)11(15)9(5-10)7-14/h4-7,15H,1-3H3
SMILES string
CC(C)(C)c1cc(C=O)c(O)c(C=O)c1
InChI key
WQNTWZJPCLUXQC-UHFFFAOYSA-N
assay
96%
mp
99-103 °C (lit.)
functional group
aldehyde
Quality Level
General description
4-tert-Butyl-2,6-diformylphenol can be prepared from 4-tert-butylphenol and hexamethylenetetramine.
Application
4-tert-Butyl-2,6-diformylphenol may be used to synthesize:
- symmetrical macrocyclic Schiff′s base
- 2,6-bis(N-(4′-methyl-2′-hydroxyphenyl)iminomethyl)-4-tert-butylphenol
- isostructural C3-symmetrical triple stranded dinuclear lanthanide analogs
- 5-tert-butyl-2 hydroxy-isophthalaldehyde-bis-2-pyridinehydrazone via reaction with 2-hydrazinopyridine
- 5-tert-butyl-2-hydroxyisophthalaldehyde-bisphenylhydrazone via reaction with phenylhydrazine
signalword
Warning
hcodes
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
Mono-and diformylation of 4-substituted phenols: a new application of the Duff reaction.
Lindoy LF, et al.
Synthesis, 07, 1029-1032 (1998)
Alternating copolymerization of carbon dioxide and epoxide by dinuclear zinc Schiff base complex.
Sugimoto H and Ogawa A.
Reactive functional Polymers, 67(11), 1277-1283 (2007)
Binuclear and polynuclear transition metal complexes with macrocyclic ligands. 2. New macrocyclic Schiff" s base in the reaction of 4-tert-butyl-2, 6-diformylphenol with 1, 2-diaminobenzene. Synthesis and structural, spectroscopic, and theoretical study.
Ustynyuk YA, et al.
Russian Chemical Bulletin, 51(3), 488- 498 (2002)
"A ?turn-on? fluorescent chemosensor for zinc ion with facile synthesis and application in live cell imaging"
Wang XLK and Tong A
Analytica Chimica Acta, 776, 69- 73 (2013)
Eswaran Chinnaraja et al.
Inorganic chemistry, 58(7), 4465-4479 (2019-04-02)
The ligand L1 of 4-methyl-2,6-diformylphenol and L2 of 4- tert-butyl-2,6-diformylphenol are synthesized through Schiff base condensation with rac-, ( R)-(+), or ( S)-(-)-1,1'-binaphthyl-2,2'-diamine (BNDA). As a result, the racemic L1rac, L2rac, and enantiopure L1RR, L1SS, L2RR, and L2SS ligands are
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