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methyl 3-chlorotricyclo[3.3.1.1~3,7~]decane-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103549-35-5

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103549-35-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103549-35-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,5,4 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103549-35:
(8*1)+(7*0)+(6*3)+(5*5)+(4*4)+(3*9)+(2*3)+(1*5)=105
105 % 10 = 5
So 103549-35-5 is a valid CAS Registry Number.

103549-35-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-chloroadamantane-1-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 3-chloroadamantyl-1-carboxylate

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:103549-35-5 SDS

103549-35-5Downstream Products

103549-35-5Relevant academic research and scientific papers

Chlorination of Adamantane and Its Derivatives by Carbon Tetrachloride in the Presence of Manganese-, Vanadium-, and Molybdenum-containing Catalysts

Khusnutdinov,Shchadneva,Baiguzina,Lavrent'eva,Burangulova,Dzhemilev

, p. 126 - 133 (2007/10/03)

The feasibility of catalytic chlorination of adamantane and its derivatives by carbon tetrachloride in the presence of manganese-, vanadium-, and molybdenum-containing catalysts activated by nitrile ligands or alcohols was established. The optimum molar ratios of catalyst components and reactants and the optimum reaction conditions for selective syntheses of mono-, di-, and trichlorosubstituted adamantane derivatives with high yields were found.

Synthese de quelques structures encombrees derivees de l'adamantane et de ses analogues par alkylation des ether d'enol trimethylsilyliques

Dubois, Jacques-Emile,Lebbar, Kadija,Lion, Claude,Dugast, Jean-Yves

, p. 905 - 910 (2007/10/02)

Alkylation of trimethylsilyl enol ethers of 2,4-dimethyl-3-pentanone, cyclopentanone and cyclohexanone has been extended to alkylating agents with a cage structure (substituted or functionalized adamantyl, diamantyl, homoadamantyl and noradamantyl chlorides or bromides).This method affords some new cage structured aliphatic and alicyclic ketones.In some cases one observes a new TiCl4 promoted reaction where the bromine in the alkylating agent is replaced by chlorine.This work is a generalization of our previous extended studies on α-alkylation of ketones with tertiary alkylating agents.

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