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31898-14-3

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31898-14-3 Usage

General Description

Tricyclo[3.3.1.1(3,7)]decane-1,3-diacetyl dichloride is a chemical compound with the molecular formula C14H18Cl2O2. It is a derivative of tricyclo[3.3.1.1(3,7)]decane, which is a fused-ring hydrocarbon structure. Tricyclo[3.3.1.1(3,7)]decane-1,3-diacetyl dichloride is a diacetyl derivative, meaning it contains two acetyl groups. Additionally, it also contains two chlorine atoms. It is commonly used as a reagent in organic synthesis and can be utilized in the preparation of various other chemical compounds. Its unique structure and functional groups make it useful in a variety of chemical reactions to produce a wide range of products.

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

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