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Tricyclo[3.3.1.1(3,7)]decane-1,3-diacetyl dichloride is a chemical compound characterized by its molecular formula C14H18Cl2O2. It is a derivative of tricyclo[3.3.1.1(3,7)]decane, which features a fused-ring hydrocarbon structure. Tricyclo[3.3.1.1(3,7)]decane-1,3-diacetyl dichloride is distinguished by the presence of two acetyl groups and two chlorine atoms, which contribute to its unique properties and reactivity in chemical reactions.

31898-14-3

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31898-14-3 Usage

Uses

Used in Organic Synthesis:
Tricyclo[3.3.1.1(3,7)]decane-1,3-diacetyl dichloride is employed as a reagent in organic synthesis for its ability to participate in a variety of chemical reactions. Its unique structure and functional groups, including the acetyl and chlorine atoms, make it a versatile building block for the preparation of a diverse array of chemical compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Tricyclo[3.3.1.1(3,7)]decane-1,3-diacetyl dichloride is used as an intermediate in the synthesis of complex organic molecules, including potential drug candidates. Its reactivity and structural features facilitate the creation of new compounds with specific therapeutic properties.
Used in Chemical Research:
Tricyclo[3.3.1.1(3,7)]decane-1,3-diacetyl dichloride is also utilized in chemical research as a model compound to study the effects of structural modifications on the reactivity and properties of organic molecules. This helps in understanding the fundamental principles of organic chemistry and can lead to the development of new synthetic methods and applications.
Used in Material Science:
In material science, Tricyclo[3.3.1.1(3,7)]decane-1,3-diacetyl dichloride can be used as a precursor to develop new materials with specific properties, such as polymers with tailored characteristics for use in various industries, including electronics, automotive, and aerospace.
Overall, the applications of Tricyclo[3.3.1.1(3,7)]decane-1,3-diacetyl dichloride are diverse, spanning across multiple industries, and are driven by its unique structural features and reactivity in chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 31898-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,8,9 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 31898-14:
(7*3)+(6*1)+(5*8)+(4*9)+(3*8)+(2*1)+(1*4)=133
133 % 10 = 3
So 31898-14-3 is a valid CAS Registry Number.

31898-14-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[3-(2-chloro-2-oxoethyl)-1-adamantyl]acetyl chloride

1.2 Other means of identification

Product number -
Other names 1,3-Adamantan-diacetylchlorid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:31898-14-3 SDS

31898-14-3Relevant articles and documents

Design and synthesis of new adamantyl-substituted antileishmanial ether phospholipids

Papanastasiou, Ioannis,Prousis, Kyriakos C.,Georgikopoulou, Kalliopi,Pavlidis, Theofilos,Scoulica, Effie,Kolocouris, Nicolas,Calogeropoulou, Theodora

, p. 5484 - 5487 (2010)

A series of new 2-[3-(2-alkyloxy-ethyl)-adamantan-1-yl]-ethoxy substituted ether phospholipids was synthesized and their antileishmanial activity was evaluated against Leishmania infantum amastigotes. The majority of the new analogues were significantly l

1,3-Adamantane-3,13-Porphyrin-6,6-Cyclophane: Crystal Structure of the Free Base and Steric Effects on Ligation of the Iron(II) Complex

Traylor, T. G.,Koga, N.,Deardruff, L. A.,Sweptson, Paul N.,Ibers, James A.

, p. 5132 - 5143 (2007/10/02)

The coupling of 1,3-adamantanediacetyl chloride to 8,18-bis(2-carbobenzoxyethyl)3-13-bis(o-aminopropyl)-2,7,12,17-tetramethylporphyrin affords 1,3-adamantane-3,13-porphyrin-6,6-cyclophane.The material crystallizes as the bis(dichloromethane)solvate, C64H7

THE CURTIUS REARRANGEMENT IN THE SERIES OF ADAMANTANE DERIVATIVES

Khardin, A. P.,Gureev, N. G.,Radchenko, S. S.

, p. 57 - 58 (2007/10/02)

1-Adamantyl isocyanate, 1,3-adamantylene diisocyanate, and 1,3-bis(isocyanatomethyl)adamantane were synthesized by the Curtius rearrangement of adamantane acyl azides.Their physicochemical characteristics were determined.

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