Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H17Cl |
| Molecular Weight | 172.695 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1(C)[C@@H]2CC[C@@]1(C)[C@@H](Cl)C2
InChI
InChIKey=XXZAOMJCZBZKPV-WEDXCCLWSA-N
InChI=1S/C10H17Cl/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8H,4-6H2,1-3H3/t7-,8+,10+/m1/s1
| Molecular Formula | C10H17Cl |
| Molecular Weight | 172.695 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Bornyl chloride is a terpene compound found in essential oils of some plants. Bornyl chloride is an intermediate in the synthetic route for camphor production. It can be obtained by hydrochlorination of alpha-Pinene, a compound found in oils of many coniferous trees. Bornyl chloride was used as an antiseptic and disinfectant.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Baseline survey of concentrations of toxaphene congeners in fish from European waters. | 2004 Aug |
|
| Structure of the toxaphene compound 2,5-endo,6-exo,8,9,9,10,10-octachlorobornene-2: a temperature-dependent formation of two rotamers. | 2005 Mar 15 |
|
| Successful computational modeling of isobornyl chloride ion-pair mechanisms. | 2010 Aug 6 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:55:13 GMT 2023
by
admin
on
Fri Dec 15 15:55:13 GMT 2023
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| Record UNII |
JXL3Y7EPZB
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