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(1S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,5-dione is a complex organic compound with the molecular formula C10H14O2. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it belongs to the class of bicyclic compounds. This specific compound features a bicyclo[2.2.1]heptane core structure, which consists of two carbon rings fused together, with the carbon atoms numbered from 1 to 7. The compound has three methyl groups attached to the carbon atoms at positions 1, 7, and 7, and two carbonyl groups (C=O) at positions 2 and 5. The stereochemistry at positions 1 and 4 is designated as S, indicating that the substituents at these positions are arranged in a specific three-dimensional orientation. (1S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,5-dione is known for its unique structural properties and potential applications in various chemical and pharmaceutical contexts.

2758-63-6

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2758-63-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2758-63-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,5 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2758-63:
(6*2)+(5*7)+(4*5)+(3*8)+(2*6)+(1*3)=106
106 % 10 = 6
So 2758-63-6 is a valid CAS Registry Number.

2758-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S)-5-oxocamphor

1.2 Other means of identification

Product number -
Other names 2,5-bornanedione

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:2758-63-6 SDS

2758-63-6Upstream product

2758-63-6Relevant academic research and scientific papers

A chromium-free synthesis of enantiopure 5-oxoborneol

Tartaggia, Stefano,Padovan, Pierluigi,Borsato, Giuseppe,De Lucchi, Ottorino,Fabris, Fabrizio

, p. 4478 - 4480 (2011)

Enantiopure (-)-5-oxoborneol was obtained in 35% overall yield in two steps, starting from readily available (-)-bornyl acetate and using oxone as a safe and inexpensive oxidant. The reported procedure avoids the use of large excess of noxious chromium(VI), which was required by the so far reported syntheses.

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