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Isobornyl chloride, also known as 1-chloro-1,7,7-trimethylbicyclo[2.2.1]heptane, is an organic compound with the chemical formula C10H17Cl. It is a colorless liquid with a pungent odor and is used as a precursor in the synthesis of various chemicals, including camphor derivatives and isobornyl acrylate. Isobornyl chloride is produced by the chlorination of camphene, a monoterpene found in the essential oils of several plants. It is an important intermediate in the production of isobornyl acrylate, which is used as a monomer in the synthesis of polymers and copolymers with unique properties, such as high transparency and resistance to UV radiation. Due to its reactivity and potential health and environmental risks, isobornyl chloride is classified as a hazardous substance and requires proper handling and disposal.

559-45-5

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559-45-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 559-45-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 559-45:
(5*5)+(4*5)+(3*9)+(2*4)+(1*5)=85
85 % 10 = 5
So 559-45-5 is a valid CAS Registry Number.

559-45-5SDS

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 DL-bornyl chloride

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:559-45-5 SDS

559-45-5Relevant academic research and scientific papers

An unprecedented elimination-driven migration: The reductive dihalobornane-camphene rearrangement

Garamszegi, Laszlo,Schlosser, Manfred

, p. 3173 - 3175 (2007/10/03)

An organometallic counterpart of the Wagner-Meerwein rearrangement, the incarnation of an carbocationic alkyl 1,2-migration, has now been discovered. However, the structural reorganization does not occur through carbanionic intermediates, but can only be brought about by a push-pull process via 1a (see scheme).

PRENYLATION OF CAMPHENE - A CARBOCATIONIC ROUTE TO ISOSANTALENE AND ITS DERIVATIVES

Rahman, Azizur,Baeuml, Englbert,Klein, Herbert,Mayr, Herbert

, p. 4119 - 4124 (2007/10/02)

Camphene 1 is converted into 8-chloromethylcamphene 3 via Prins reaction.Treatment of 3 with zinc chloride/ether in the presence of isobutene gives the 1:1 adduct 11, from which isosantalene 7, its isomer 6, and the corresponding alcohol 5 are obtained.

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