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2-Allylbicyclo[2.2.1]heptane is a cyclic hydrocarbon compound with the molecular formula C10H16. It features a bicyclic structure with a seven-membered ring and an allyl group attached to the second carbon atom. This organic compound is known for its unique shape and properties, which arise from the fusion of two rings and the presence of a double bond in the allyl group. It is an important building block in organic synthesis, particularly for the preparation of various natural products and pharmaceuticals, due to its ability to undergo a range of chemical reactions, such as Diels-Alder reactions, which can lead to the formation of complex molecular structures. The compound's stability and reactivity make it a valuable intermediate in the synthesis of a wide array of organic compounds.

2633-80-9

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2633-80-9 Usage

Classification

Terpene

Physical state

Colorless liquid

Odor

Camphor-like

Uses

Building block in pharmaceutical synthesis, starting material for fragrances and flavoring agents

Potential applications

Organic chemistry, drug development

Check Digit Verification of cas no

The CAS Registry Mumber 2633-80-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,3 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2633-80:
(6*2)+(5*6)+(4*3)+(3*3)+(2*8)+(1*0)=79
79 % 10 = 9
So 2633-80-9 is a valid CAS Registry Number.

2633-80-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-prop-2-enylbicyclo[2.2.1]heptane

1.2 Other means of identification

Product number -
Other names 2-Allylbicyclo<2.2.1>heptan

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:2633-80-9 SDS

2633-80-9Downstream Products

2633-80-9Relevant academic research and scientific papers

Direct substitution of the hydroxy group in alcohols with silyl nucleophiles catalyzed by indium trichloride

Yasuda, Makoto,Saito, Takahiro,Ueba, Masako,Baba, Akio

, p. 1414 - 1416 (2007/10/03)

Straightforward substitution: An excellent combination of a silyl nucleophile and indium catalyst was used to accomplish the dehydroxylation/ alkylation of alcohols under nearly neutral conditions (see scheme, Si = silyl group) even though this type of reaction usually requires at least an equimolar amount of acid.

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