1,3-Adamantanedicarbonyl chloride

  • Name: 1,3-Adamantanedicarbonyl chloride
  • CAS: 29713-15-3
  • Purity: 99%
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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

adamantane-1,3-dicarboxylic acid
39269-10-8

adamantane-1,3-dicarboxylic acid

1,3-adamantanedicarbonyl chloride
29713-15-3

1,3-adamantanedicarbonyl chloride

Conditions
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;
1,3-adamantanedicarbonyl chloride
29713-15-3

1,3-adamantanedicarbonyl chloride

Conditions
Conditions Yield
With thionyl chloride;

29713-15-3 Upstream products

  • 39269-10-8
    39269-10-8

    adamantane-1,3-dicarboxylic acid

  • 828-51-3
    828-51-3

    1-Adamantanecarboxylic acid

  • 39269-10-8
    39269-10-8

    adamantane-1,3-dicarboxylic acid

29713-15-3 Downstream products

  • 62472-39-3
    62472-39-3

    1,3-adamantane-dicarbonamide

  • 167902-36-5
    167902-36-5

    1,3-dibenzoyldadamantane

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