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3-(1-adamantyloxy)propan-1-amine is a complex chemical compound that belongs to the class of organic compounds known as adamantanes, which are compounds containing the adamantane moiety, a polycyclic saturated hydrocarbon made up of three condensed cyclohexane rings. The chemical structure features an adamantyl group bonded through an oxygen atom to a 3-carbon chain that ends in an amine functional group.

21624-07-7

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21624-07-7 Usage

Uses

Used in Scientific Research:
3-(1-adamantyloxy)propan-1-amine is used as a research compound for its unique structural configuration that can be utilized in the formation of more complex molecules and potential drugs.
Used in Pharmaceutical Research:
3-(1-adamantyloxy)propan-1-amine is used as a building block in the development of new pharmaceuticals, due to its potential to contribute to the synthesis of novel drug candidates. It is not typically found in nature but is synthesized in laboratories for specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 21624-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,2 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 21624-07:
(7*2)+(6*1)+(5*6)+(4*2)+(3*4)+(2*0)+(1*7)=77
77 % 10 = 7
So 21624-07-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H23NO/c14-2-1-3-15-13-7-10-4-11(8-13)6-12(5-10)9-13/h10-12H,1-9,14H2

21624-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1-Adamantyloxy)propan-1-amine

1.2 Other means of identification

Product number -
Other names 1-(3-aminopropoxy)adamantane

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:21624-07-7 SDS

21624-07-7Downstream Products

21624-07-7Relevant academic research and scientific papers

Chemical Transformations of Tetracyclo[3.3.1.13,7.01,3]decane (1,3-Dehydroadamantane): VII. Reaction of 1,3-Dehydroadamantane with Alkanediols and Amino Alcohols

Butov,Mokhov

, p. 1760 - 1763 (2019/03/26)

The reaction of 1,3-dehydroadamantane with C2–C6 α,ω-alkanediols selectively afforded ω-(adamantan- 1-yloxy)alkan-1-ols in 87–94% yield. The reaction of 1,3-dehydroadamantane with ω-aminoalkan-1- ols (2-aminoethanol and 3-aminopropan-1-ol) gave mixtures of addition products through the oxygen and nitrogen atoms, which can be readily separated by fractional vacuum distillation or crystallization.

DERIVATIVES OF ADAMANTANE. I. 2-HYDROXYETHYLAMINO DERIVATIVES OF ADAMANTANE

Plakhotnik, V. M.,Kovtun, V. Yu.,Krasutskii, P. A.,Novikova, M. I.,Prokhorov, A. B.,et al.

, p. 1287 - 1290 (2007/10/02)

The reaction of 1-bromoadamantane with hydroxyalkylamines leads to the preferential formation of 1-(aminoalkoxy)adamantanes.The 2-hydroxyethylamino derivatives of the adamantane series were obtained by the reaction of ethylene oxide with the corresponding amines.

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