1,3-Adamantanedicarbonyl chloride
- Name: 1,3-Adamantanedicarbonyl chloride
- CAS: 29713-15-3
- Purity: 99%
Details
Chinese Manufacturer supply 1,3-Adamantanedicarbonyl chloride 29713-15-3 in stock with high standard
- Molecular Formula: C12H14Cl2O2
- Molecular Weight: 261.148
- Vapor Pressure: 0.000372mmHg at 25°C
- Melting Point: 89-90 °C
- Refractive Index: 1.586
- Boiling Point: 318 °C at 760 mmHg
- Flash Point: 161 °C
- PSA: 34.14000
- Density: 1.441 g/cm3
- LogP: 3.10380
1,3-Adamantanedicarbonyl chloride(Cas 29713-15-3) Usage
|
General Description |
1,3-Adamantanedicarbonyl chloride is a chemical compound with the molecular formula C13H18Cl2O2. It is a derivative of adamantane and belongs to the class of organic compounds known as carbonyl compounds, which are organic compounds containing a carbon-oxygen double bond. 1,3-Adamantanedicarbonyl chloride is a colorless liquid with a high boiling point and is commonly used as a reagent in organic synthesis reactions. It is a versatile building block for the chemical industry and is utilized in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, 1,3-Adamantanedicarbonyl chloride has potential applications in the fields of material science and nanotechnology due to its unique molecular structure and reactivity. |
InChI:InChI=1/C12H14Cl2O2/c13-9(15)11-2-7-1-8(4-11)5-12(3-7,6-11)10(14)16/h7-8H,1-6H2
29713-15-3 Relevant articles
Synthesis, physiochemical property and antibacterial activity of gemini quaternary ammonium salts with a rigid spacer
Fu,Guo,Zhong,Yang,Lai
, p. 16507 - 16515 (2016)
A novel series of adamantane-based gemin...
Synthesis, surface property and antimicrobial activity of cationic gemini surfactants containing adamantane and amide groups
Zhong, Xing,Guo, Jianwei,Fu, Shuqin,Zhu, Dongyu,Peng, Jinping
, p. 943 - 950 (2014)
A series of novel cationic gemini surfac...
A photosensitive semi-alicyclic poly(benzoxazole) with high transparency and low dielectric constant
Fukukawa, Ken-Ichi,Shibasaki, Yuji,Ueda, Mitsuru
, p. 8256 - 8261 (2004)
A photosensitive semi-alicyclic poly(ben...
Preparation of diisocyanates of adamantane and diamantane
Davis, Matthew C.,Dahl, Jeremy E. P.,Carlson, Robert M. K.
, p. 1153 - 1158 (2008)
The 1,6- and 4,9-diisocyanates of diaman...
Aziridine-2-carboxylic acid derivatives and its open-ring isomers as a novel PDIA1 inhibitors
Leite, Irena,Andrianov, Victor,Zelencova-Gopejenko, Diana,Loza, Einars,Kazhoka-Lapsa, Iveta,Domracheva, Ilona,Stoyak, Marta,Chlopicki, Stefan,Kalvins, Ivars
, p. 1086 - 1106 (2022/01/12)
[Figure not available: see fulltext.] Ac...
Four-Directional synthesis of adamantane derivatives
Qu, Tao,White, Andrew J. P.,Barrett, Anthony G. M.
, p. 18 - 50 (2020/08/28)
1-Adamantanemethanol, 1,3-adamantanedime...
Synthesis method and application of compound methyl 5-fluorouracil adamantane carboxylate
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Paragraph 0023; 0028-0029, (2019/11/29)
The invention discloses a synthesis meth...
CYCLIC PEPTIDES MULTIMERS TARGETING α4β7 INTEGRIN
-
Page/Page column 29; 30; 106, (2018/05/27)
There is described herein, multimers com...
29713-15-3 Process route
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39269-10-8
adamantane-1,3-dicarboxylic acid
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29713-15-3
1,3-adamantanedicarbonyl chloride
| Conditions | Yield |
|---|---|
|
With
thionyl chloride;
|
99%
|
|
With
thionyl chloride;
at 20 - 95 ℃;
for 6h;
|
93%
|
|
With
thionyl chloride;
Heating;
|
|
|
With
thionyl chloride;
for 2h;
Yield given;
Heating;
|
|
|
With
thionyl chloride;
|
|
|
With
thionyl chloride;
In
chloroform;
at 0 - 25 ℃;
|
|
|
With
thionyl chloride;
In
N,N-dimethyl-formamide;
|
|
|
With
thionyl chloride;
for 6h;
Heating;
|
|
|
With
thionyl chloride;
Reflux;
|
|
|
With
thionyl chloride;
for 3h;
Reflux;
|
|
|
With
oxalyl dichloride; N,N-dimethyl-formamide;
In
dichloromethane;
at 20 ℃;
for 21h;
Inert atmosphere;
|
|
|
With
oxalyl dichloride;
In
dichloromethane; N,N-dimethyl-formamide;
at 20 ℃;
for 21h;
Inert atmosphere;
|
|
|
With
thionyl chloride;
for 4h;
Reflux;
|
|
|
With
thionyl chloride;
for 4h;
Reflux;
Inert atmosphere;
|
|
|
With
thionyl chloride; N,N-dimethyl-formamide;
In
chloroform;
at 75 ℃;
|
|
|
With
thionyl chloride;
In
dichloromethane;
at 20 - 70 ℃;
|
|
|
With
thionyl chloride;
In
N,N-dimethyl-formamide;
at 70 ℃;
for 5h;
|
|
|
With
thionyl chloride;
for 2h;
Reflux;
Inert atmosphere;
|
11.7 g
|
|
With
oxalyl dichloride; N,N-dimethyl-formamide;
In
dichloromethane;
at 20 ℃;
for 2h;
|
-
-
29713-15-3
1,3-adamantanedicarbonyl chloride
| Conditions | Yield |
|---|---|
|
With
thionyl chloride;
|
29713-15-3 Upstream products
-
39269-10-8
adamantane-1,3-dicarboxylic acid
-
828-51-3
1-Adamantanecarboxylic acid
-
39269-10-8
adamantane-1,3-dicarboxylic acid
29713-15-3 Downstream products
-
62472-39-3
1,3-adamantane-dicarbonamide
-
167902-36-5
1,3-dibenzoyldadamantane
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