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3-Acetoxytricyclo[2.2.1.02,6]heptane is a complex organic compound with the molecular formula C10H16O2. It is a member of the tricycloheptane family, characterized by its three-ring structure. 3-Acetoxytricyclo[2.2.1.02,6]heptane features a 3-acetoxy group, which is an acetate ester functional group attached to one of the carbon atoms in the heptane chain. The acetoxy group is an ester derived from acetic acid, indicating that the compound has potential reactivity with nucleophiles and can undergo hydrolysis to release acetic acid and the corresponding alcohol. The structure of 3-acetoxytricyclo[2.2.1.02,6]heptane is rigid due to its cyclic nature, and it is likely to exhibit unique chemical properties and reactivity patterns compared to its acyclic counterparts. 3-Acetoxytricyclo[2.2.1.02,6]heptane may be of interest in organic synthesis, particularly in the preparation of complex molecules with specific stereochemistry or as a precursor in the synthesis of pharmaceuticals and other specialty chemicals.

6555-48-2

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6555-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6555-48-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6555-48:
(6*6)+(5*5)+(4*5)+(3*5)+(2*4)+(1*8)=112
112 % 10 = 2
So 6555-48-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O2/c1-4(10)11-9-5-2-6-7(3-5)8(6)9/h5-9H,2-3H2,1H3

6555-48-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,5,6,7-hexahydro-1H-tricyclo[2.2.1.0<sup>2,6</sup>]heptan-3-yl acetate

1.2 Other means of identification

Product number -
Other names 3-Acetoxynortricyclene

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:6555-48-2 SDS

6555-48-2Relevant academic research and scientific papers

REACTION OF ACETYL NITRATE WITH QUADRICYCLENE

Zyk, N. V.,Nikulin, A. V.,Kolbasenko, S. I.,Zefirov, N. S.

, p. 1881 - 1884 (2007/10/02)

The reaction of acetyl nitrate with tetracyclo2,7-04,6>heptane (quadricyclene) takes place in two directions with initial electrophilic attack both by the nitronium ion and by the proton, giving the series of corresponding substituted derivatives of nortricyclene.

Reaction of 2,4-Dinitrobenzenesulfenyl Chloride with Quadricyclene

Zefirov, Nikolai S.,Sadovaya, N. K.,Velikokhat'ko, T. N.,Andreeva, L. A.,Morrill, Terence C.

, p. 1468 - 1471 (2007/10/02)

The treatment of quadricyclene with 2,4-dinitrobenzenesulfenyl chloride has been reinvestigated and chloro adducts 1-A and 2b-A as well as acetates 4a-A, 4b-A, 6, and 7 have been obtained.Establishing 2b-A with endo-chloride led to important conclusion that endo-chloride attack occurs by collapse of ion pair.Monitoring changes in the proportions of acetates, especially with added LiClO4, has allowed conclusions about the degree of development of the carbocation intermediates.These conclusions were proposed on the basis of the previously published ideas of stereocontrol by an ion pair.

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