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3405-48-9

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3405-48-9 Usage

General Description

N-(1-Adamantyl)formamide is an organic compound that is derived from formamide and 1-adamantylamine. It is a white crystalline solid that is soluble in organic solvents such as methanol and ethyl acetate. N-(1-Adamantyl)formamide has a wide range of potential applications, including as a reagent in organic synthesis and as an intermediate for the production of pharmaceuticals and agrochemicals. It is also known to exhibit anti-inflammatory and anti-cancer properties and is being studied for its potential use in the treatment of various diseases. However, further research is needed to fully understand its potential benefits and risks.

Check Digit Verification of cas no

The CAS Registry Mumber 3405-48-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,0 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3405-48:
(6*3)+(5*4)+(4*0)+(3*5)+(2*4)+(1*8)=69
69 % 10 = 9
So 3405-48-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H17NO/c13-7-12-11-4-8-1-9(5-11)3-10(2-8)6-11/h7-10H,1-6H2,(H,12,13)

3405-48-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1-adamantyl)formamide

1.2 Other means of identification

Product number -
Other names N-adamantanylcarboxamide

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:3405-48-9 SDS

3405-48-9Relevant articles and documents

The Invention of Radical Reactions. 32. Radical Deoxygenations, Dehalogenations, and Deaminations with Dialkyl Phosphites and Hypophosphorous Acid as Hydrogen Sources

Barton, Derek H. R.,Jang, Doo Ok,Jaszberenyi, Joseph Cs.

, p. 6838 - 6842 (2007/10/02)

Reagents, containing a P-H bond, such as dimethyl phosphite, diethyl phosphite, hypophosphorous acid and various salts of hypophosphorous acid are effective radical reducing agents for organic halides, thionoesters, and isocyanides affording high yields of the corresponding hydrocarbons.Reduction of tertiary phenyl selenides and tertiary nitro compounds are not efficient under these conditions.Olefination of 1,2-diols is also accomplished via the corresponding thiocarbonyl derivatives using hypophosphorous acid and triethylamine in the presence of a suitable "sacrifical olefin" im moderate to good yields.

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