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2-(1-Adamantyl)propane, also known as 2-(1-adamantyl)propane-1-ol, is an organic compound with the chemical formula C13H22O. It is a colorless liquid with a molecular weight of 194.32 g/mol. 2-(1-adamantyl)propane is characterized by its adamantane-based structure, which consists of a rigid, cage-like carbon framework. The molecule features a propane chain attached to the adamantane core, with a hydroxyl group at the end of the propane chain. 2-(1-Adamantyl)propane is used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. It is also employed as a building block in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural properties and potential to influence the stereochemistry of the final products.

773-32-0

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773-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 773-32-0 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 773-32:
(5*7)+(4*7)+(3*3)+(2*3)+(1*2)=80
80 % 10 = 0
So 773-32-0 is a valid CAS Registry Number.

773-32-0SDS

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-propan-2-yladamantane

1.2 Other means of identification

Product number -
Other names isopropyl 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:773-32-0 SDS

773-32-0Downstream Products

773-32-0Relevant 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

Reductive Alkylation and Reduction of Tertiary, Secondary, and Benzylic Alcohols with Trimethyl-, Triethyl-, and Triisopropylboron/Trifluoromethanesulfonic (Triflic) Acid

Olah, George A.,Wu, An-hsiang,Farooq, Omar

, p. 2759 - 2761 (2007/10/02)

Tertiary, secondary, and benzylic alcohols were reductively alkylated and reduced with trimethyl-, triethyl-, and triisopropylboron/trifluoromethanesulfonic (triflic) acid.A postulated mechanism for the reactions is discussed.

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