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42067-67-4

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42067-67-4 Usage

General Description

AKOS BC-0207 is a chemical compound with the molecular formula C24H34N6O4S. It is primarily used as a reagent or intermediate in organic synthesis. It is known to have inhibitory effects on certain enzymes and has been suggested to have potential applications in pharmaceutical research. AKOS BC-0207 has also been studied for its potential as a treatment for various diseases and conditions, including cancer. It is important to handle this chemical with caution and follow appropriate safety protocols when working with it in a laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 42067-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,6 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42067-67:
(7*4)+(6*2)+(5*0)+(4*6)+(3*7)+(2*6)+(1*7)=104
104 % 10 = 4
So 42067-67-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H19N/c12-6-11-9-2-7-1-8(4-9)5-10(11)3-7/h7-11H,1-6,12H2

42067-67-4SDS

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-adamantylmethanamine

1.2 Other means of identification

Product number -
Other names adamantan-2-ylmethanamine

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:42067-67-4 SDS

42067-67-4Relevant articles and documents

Synthesis and Reactions of 2-Adamantylidenenitromethane

Klimochkin,Leonova,Moiseev

, p. 494 - 498 (2007/10/03)

Synthesis of 2-adamantylidenenitromethane by nitration of 2-methyl-2-adamantanol was developed. Reaction of the 2-adamantylidenenitromethane with acids HX (X = ONO2, Cl, Br) yields the corresponding 2-X-adamantane-2-carboxylic acids, and under conditions of Ritter's reaction affords 2-acetylaminoadamantane-2-carboxylic acid. Reaction of the 2-adamantylidenenitromethane with nitric acid in a mixture with acetic anhydride occurs with carcass rearrangement and results in 4-exo-nitroxy-3-protoadamantanecarboxylic acid. The reduction of the nitroolefin with lithium aluminum hydride furnishes 2-aminomethyladamantane, and reaction with excess methylmagnesium iodide gives N-(2-methyl-2-adamantyl)methyl-N-hydroxylamine.

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