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1,4,4-trichloroadamantane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38433-24-8

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38433-24-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38433-24-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,3 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38433-24:
(7*3)+(6*8)+(5*4)+(4*3)+(3*3)+(2*2)+(1*4)=118
118 % 10 = 8
So 38433-24-8 is a valid CAS Registry Number.

38433-24-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,4-trichloroadamantane

1.2 Other means of identification

Product number -
Other names -

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:38433-24-8 SDS

38433-24-8Downstream Products

38433-24-8Relevant academic research and scientific papers

Reactions of Bridged Halosubstituted Adamantane Derivatives with Nitric Acid

Klimochkin,Leonova,Moiseev,Aleksandrov

, p. 340 - 344 (2007/10/03)

Reactions of bridged halosubstituted adamantane derivatives with nitric acid result in nitrolysis products. In the presence of acetic anhydride, the reactions proceed at nodal positions to form nitroxy derivatives, while in the case of 2,2-dichloroadamantane, the formation of a 1,4,4-trichloro-substituted derivative is observed. The nitroxylation of 2-fluoroadamantane results in the formation of predominantly products with the Z-configuration.

REACTION OF ADAMANTANONE, DIAMANTANONE, AND THEIR DERIVATIVES WITH THIONYL CHLORIDE

Janku, Josef,Burkhard, Jiri,Vodicka, Ludek

, p. 2028 - 2034 (2007/10/02)

In reaction of adamantanone, diamantanone, and their chloro or oxo derivatives with thionyl chloride the oxo group is replaced with two chlorine atoms under formation of geminal dichloro derivatives.The presence of a chlorine atom or an oxo group in both ketones reduces the reaction rate.The reaction rate decreases with decreasing distance between the substituent and the carbonyl group.Ketones with chlorine atom in α- or β-axial position do not react with thionyl chloride.The reaction is accelerated by hydrogen chloride whereas in the presence of pyridine no reaction was observed.

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