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2,2-Dichloroadamantane is an organic compound with the chemical formula C10H14Cl2. It is a derivative of adamantane, a highly symmetrical and stable carbon cage structure, with two chlorine atoms attached to the 2nd carbon position. 2,2-Dichloroadamantane is known for its unique physical and chemical properties, such as high thermal stability and resistance to chemical reactions. It has potential applications in various fields, including pharmaceuticals, materials science, and as a precursor in the synthesis of other organic compounds. Due to its low reactivity, 2,2-dichloroadamantane is also considered a safer alternative to some more reactive chlorinated compounds.

7419-57-0

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7419-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7419-57-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,1 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7419-57:
(6*7)+(5*4)+(4*1)+(3*9)+(2*5)+(1*7)=110
110 % 10 = 0
So 7419-57-0 is a valid CAS Registry Number.

7419-57-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-Dichloroadamantane

1.2 Other means of identification

Product number -
Other names 2,2-dichloroadamantane

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:7419-57-0 SDS

7419-57-0Upstream product

7419-57-0Relevant academic research and scientific papers

Preparative catalytic chlorination of adamantane, cyclohexane, and hexane in the system tetrachloromethane-MX2(PPh3)2 (MX2 = PdBr2, PtCl2)-acetonitrile-potassium carbonate

Vedernikov,Sayakhov,Zazybin,Solomonov

, p. 812 - 815 (2007/10/03)

Heating of saturated hydrocarbons RH (cyclohexane, adamantane, and hexane) with tetrachloromethane in the presence of acetonitrile, potassium carbonate, and catalytic amounts of dihalide triphenylphosphine complexes of palladium(II) or platinum(II), MX2(PPh)2 (MX2 = PdBr2, PtCi2), for 6-8 h at 120°C yields monochlorinated derivatives of the respective hydrocarbons in 30-55% yield. Benzene, toluene, ethylbenzene, and tetramethylsilane show low reactivity under the conditions adopted for the reaction. Relative reactivity of various bond types C-H of alkanes is in agreement with the well known sequence: tertiary > secondary > primary. A scheme is proposed assuming trichloromethyl radicals as active species, and the catalyst function consists in activating C-C1 bond of the tetrachloromethane.

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