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Adamantyl isopropene, also known as 1-adamantyl isopropene or 1-(1-adamantyl)-2-propene, is an organic compound with the chemical formula C13H22. It is a colorless liquid at room temperature and is derived from the adamantane molecule, which is a highly stable and symmetrical hydrocarbon with a diamond-like structure. Adamantyl isopropene is characterized by its adamantane core, which provides it with unique chemical and physical properties, such as high thermal stability and resistance to chemical reactions. adamantyl isopropene is primarily used as a building block in the synthesis of various organic compounds, particularly those with complex structures, and can be found in applications ranging from pharmaceuticals to materials science.

773-33-1

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773-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 773-33-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 773-33:
(5*7)+(4*7)+(3*3)+(2*3)+(1*3)=81
81 % 10 = 1
So 773-33-1 is a valid CAS Registry Number.

773-33-1SDS

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 1-prop-1-en-2-yladamantane

1.2 Other means of identification

Product number -
Other names 1-isopropenyladamantane

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:773-33-1 SDS

773-33-1Relevant academic research and scientific papers

Reactions of 1-haloadamantanes and ethylmercury chloride with nitronate anions by the SRN1 mechanism

Santiago, Ana N.,Basso, Silvana M.,Toledo, Carlos A.,Rossi, Roberto A.

, p. 875 - 880 (2007/10/03)

Secondary or tertiary nitro compounds can be easily obtained by photostimulated reaction of the anions corresponding to primary or secondary nitroalkanes with either 1-iodoadamantane (1-AdI) or ethylmercury chloride (EtHgCl) by the SRN1 mechani

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