BENODANIL
Basic Information
- CAS No.: 15310-01-7
Physical properties
Product Description
Buy reliable Quality BENODANIL 15310-01-7 raw material with Honest Price
- Molecular Formula: C13H10 I N O
- Molecular Weight: 323.133
- Vapor Pressure: 0.000266mmHg at 25°C
- Melting Point: 144-146℃
- Refractive Index: 1.7010 (estimate)
- Boiling Point: 323.2°Cat760mmHg
- PKA: 12.87±0.70(Predicted)
- Flash Point: 149.3°C
- PSA： 29.10000
- Density: 1.697g/cm3
- LogP: 3.61650
BENODANIL(Cas 15310-01-7) Usage
|
Definition |
ChEBI: A member of the class of benzamides, obtained by formal condensation of the carboxy group of 2-iodobenzoic acid with the amino group of aniline. An obsolete fungicide once used mainly to control rust diseases. |
InChI:InChI=1/C13H10INO/c14-12-9-5-4-8-11(12)13(16)15-10-6-2-1-3-7-10/h1-9H,(H,15,16)
15310-01-7 Relevant articles
Inhibition of Pseudomonas aeruginosa Alginate Synthesis by Ebselen Oxide and Its Analogues
Kim, Soo-Kyoung,Ngo, Huy X.,Dennis, Emily K.,Thamban Chandrika, Nishad,Deshong, Philip,Garneau-Tsodikova, Sylvie,Lee, Vincent T.
, p. 1713 - 1726 (2021)
Pseudomonas aeruginosa is a Gram-negativ...
Visible-light-induced direct construction of amide bond from carboxylic acids with amines in aqueous solution
Wang, Jin,Hou, Huiqing,Hu, Yongzhi,Lin, Jin,Wu, Min,Zheng, Zhiqiang,Xu, Xiuzhi
supporting information, (2021/02/09)
A novel visible-light-promoted N-acylati...
The Mpro structure-based modifications of ebselen derivatives for improved antiviral activity against SARS-CoV-2 virus
Jin, Lin,Luo, Jiajie,Qiao, Zhen,Wang, KeWei,Wei, Ningning,Zhang, Hongyi,Zhang, Yanru
, (2021/11/09)
The main protease (Mpro or 3CLpro) of SA...
Convenient synthesis of benziodazolone: New reagents for direct esterification of alcohols and amidation of amines
Postnikov, Pavel S.,Rohde, Gregory T.,Saito, Akio,Shea, Michael T.,Vlasenko, Yulia A.,Yoshimura, Akira,Yusubov, Mekhman S.,Zhdankin, Viktor V.
, (2021/12/17)
Hypervalent iodine heterocycles represen...
15310-01-7 Process route
-
-
88-67-5
2-Iodobenzoic acid
-
-
62-53-3
aniline
-
-
15310-01-7
benodanil
| Conditions | Yield |
|---|---|
|
2-Iodobenzoic acid;
With
thionyl chloride;
for 7h;
Reflux;
aniline;
at 0 ℃;
|
98%
|
|
2-Iodobenzoic acid;
With
thionyl chloride;
for 7h;
Reflux;
aniline;
at 0 ℃;
|
93%
|
|
With
dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride;
In
tetrahydrofuran; dichloromethane;
at 20 ℃;
|
92%
|
|
2-Iodobenzoic acid;
With
thionyl chloride; triethylamine;
In
dichloromethane;
at 0 ℃;
for 0.25h;
Inert atmosphere;
aniline;
In
dichloromethane;
at 0 ℃;
Inert atmosphere;
|
88%
|
|
With
tetrabutylammomium bromide; caesium carbonate;
In
water;
at 20 ℃;
for 0.5h;
chemoselective reaction;
Electrochemical reaction;
|
87%
|
|
With
tetrabutylammomium bromide; iodine; potassium hydroxide;
In
water;
at 20 ℃;
for 2.5h;
Irradiation;
|
85%
|
|
With
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride;
In
dichloromethane;
|
18%
|
|
2-Iodobenzoic acid;
With
dmap; dicyclohexyl-carbodiimide;
In
dichloromethane;
for 1h;
aniline;
In
dichloromethane;
at 20 ℃;
|
|
|
With
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride;
In
tetrahydrofuran; dichloromethane;
at 25 ℃;
for 12h;
|
-
-
609-67-6
2-Iodobenzoyl chloride
-
-
15310-01-7
benodanil
| Conditions | Yield |
|---|---|
|
With
triethylamine hydrochloride; triethylamine; aniline;
In
water; benzene;
|
98%
|
15310-01-7 Upstream products
-
609-67-6
2-Iodobenzoyl chloride
-
62-53-3
aniline
-
88-67-5
2-Iodobenzoic acid
-
118-92-3
anthranilic acid
15310-01-7 Downstream products
-
26260-02-6
2-iodobenzaldehyde
-
5866-74-0
(2-Iodo-benzoyl)-phenyl-carbamic acid isopropyl ester
-
93-98-1
N-phenyl benzoyl amide
-
82945-16-2
2-aminobenzophenone hydroiodide