56990-02-4
- Product Name：3,5-Dibromoanthranilaldehyde
- Molecular Formula：C7H4Br2O
- Purity：99%
- Molecular Weight：263.916
Product Details
pd_meltingpoint:84-88 °C(lit.)
Appearance:White powder
Purity:99%
Good factory exports good 3,5-Dibromoanthranilaldehyde 56990-02-4
- Molecular Formula:C7H4Br2O
- Molecular Weight:263.916
- Appearance/Colour:White powder
- Melting Point:84-88 °C(lit.)
- Boiling Point:287.221 °C at 760 mmHg
- Flash Point:113.496 °C
- PSA：17.07000
- Density:1.977 g/cm3
- LogP:3.02410
56990-02-4 Relevant articles
Alkyl-thiophene Functionalized D-π-A Porphyrins for Mesoscopic Solar Cells
Lu, Jianfeng,Liu, Shuangshuang,Shen, Yan,Xu, Jie,Cheng, Yibing,Wang, Mingkui
, p. 187 - 196 (2015)
An alkyl-thiophene functionalized D-π-A ...
Synthesis, photoluminescence, and electroluminescence characterization of double tetraphenylethene-tethered BODIPY luminogens
Yang, Chiun-Jen,Lee, Jian Haur,Chen, Chin-Ti
, p. 1199 - 1210 (2019)
Three double tetraphenylethene (TPE)-tet...
Synthesis of new Zn (II) complexes for photo decomposition of organic dye pollutants, industrial wastewater and photo-oxidation of methyl arenes under visible-light
Ahemed, Jakeer,Bhongiri, Yadagiri,Chetti, Prabhakar,Gade, Ramesh,Kore, Ranjith,Pasha, Jakeer,Pola, Someshwar,Rao D, Venkateshwar
, (2021/07/28)
Synthesis of new Schiff's base Zn-comple...
Meso-substituted boron-dipyrromethene compounds: synthesis, tunable solid-state emission, and application in blue-driven LEDs
Liu, Hao,Su, Huan,Chen, Zhiyuan,Zhu, Senqiang,Liu, Rui,Zhu, Hongjun
, p. 1697 - 1705 (2021/07/10)
In this work, we depict the synthesis an...
Stable and efficient phosphorescent organic light-emitting device utilizing a δ-carboline-containing host displaying thermally activated delayed fluorescence
Liu, Shihao,Wang, Hui,Xie, Wenfa,Zang, Chunxiu,Zhang, Letian,Zhao, Hongyu
, p. 3800 - 3806 (2020/03/31)
Materials displaying thermally activated...
56990-02-4 Process route
-
-
1611-92-3
3,5-dibromotoluene
-
-
56990-02-4
3,5-dibromobenzaldehyde
| Conditions | Yield |
|---|---|
|
With
C15H11ClN4SZn; p-benzoquinone;
In
tert-butyl alcohol;
for 8h;
Reagent/catalyst;
|
83% |
|
With
bromine;
at 180 - 200 ℃;
Erwaermen des Reaktionsprodukts mit konz. Schwefelsaeure auf 70-80grad;
|
|
|
Multi-step reaction with 2 steps
1: dibenzoyl peroxide; N-Bromosuccinimide / tetrachloromethane / 24 h / Reflux
2: 4-methylmorpholine N-oxide / tetrahydrofuran / 12 h / Reflux
With
N-Bromosuccinimide; 4-methylmorpholine N-oxide; dibenzoyl peroxide;
In
tetrahydrofuran; tetrachloromethane;
|
-
-
56908-88-4
3,5-dibromobenzyl bromide
-
-
56990-02-4
3,5-dibromobenzaldehyde
| Conditions | Yield |
|---|---|
|
With
4-methylmorpholine N-oxide;
In
tetrahydrofuran;
for 12h;
Reflux;
|
92% |
56990-02-4 Upstream products
-
1611-92-3
3,5-dibromotoluene
-
42460-62-8
4-amino-3,5-dibromo-benzaldehyde
-
108-24-7
acetic anhydride
-
626-39-1
1,3,5-trisbromobenzene
56990-02-4 Downstream products
-
153390-73-9
3,5‐bis((trimethylsilyl)ethynyl)benzaldehyde
-
56988-17-1
C15H9Br2NO4
-
120359-56-0
3,5-dibromostyrene
-
145691-59-4
(3,5-dibromophenyl)methanol
Relevant Products
-
4-Bromobenzoic acidCAS：586-76-5
-
9-FluorenoneCAS：486-25-9
-
Bis(4-(tert-butyl)phenyl)(phenyl)sulfonium chloride
CAS：1931948-34-3
