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CAS No.: | 507-70-0 |
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Name: | Borneol |
Article Data: | 192 |
Cas Database | |
Molecular Structure: | |
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Formula: | C10H18O |
Molecular Weight: | 154.252 |
Synonyms: | Bicyclo[2.2.1]heptan-2-ol,1,7,7-trimethyl-, endo-;Borneol (8CI);2-Borneol;2-endo-Bornyl alcohol;Camphol;NSC 60223;dl-Borneol;endo-2-Hydroxy-1,7,7-trimethylnorbornane;endo-Borneol;rel-(1S,2R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol; |
EINECS: | 208-080-0 |
Density: | 0.992 g/cm3 |
Melting Point: | 206-209 °C |
Boiling Point: | 212 °C at 760 mmHg |
Flash Point: | 65.6 °C |
Solubility: | insoluble in water |
Appearance: | solid |
Hazard Symbols: |
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Risk Codes: | 11-43-22 |
Safety: | 16-36/37 |
Transport Information: | UN 1312 4.1/PG 3 |
PSA: | 20.23000 |
LogP: | 2.19350 |
1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one
1,7,7-trimethyl bicyclo[2.2.1]heptan-2-ol
Conditions | Yield |
---|---|
With sodium tetrahydroborate; water; titanium(IV) oxide at 20℃; for 1h; regioselective reaction; | 98% |
With hydrogenchloride; K9-OThx-9-BBNH) In tetrahydrofuran at 0℃; Product distribution; stereoselectivity, other boranes; | 97.5% |
With Triethoxysilane; cesium fluoride at 25℃; for 0.0166667h; | 95% |
1,7,7-trimethyl bicyclo[2.2.1]heptan-2-ol
Conditions | Yield |
---|---|
With silica triflate In methanol for 0.333333h; Heating; | 93% |
Borneol, trimethylsilyl ether
1,7,7-trimethyl bicyclo[2.2.1]heptan-2-ol
Conditions | Yield |
---|---|
With silica triflate In methanol for 0.0666667h; Heating; | 90% |
With methanol at 20℃; for 0.916667h; | 89% |
With ammonium chloride In water; acetonitrile at 80℃; for 1.5h; | 83% |
Conditions | Yield |
---|---|
With iron(III) perchlorate for 3h; Ambient temperature; | 85% |
dichloromethane
1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one
A
2-methylenebornane
B
1,7,7-trimethyl bicyclo[2.2.1]heptan-2-ol
Conditions | Yield |
---|---|
With titanium tetrachloride; magnesium In tetrahydrofuran at 0 - 20℃; for 1h; | A 74% B n/a |
ethanol
toluene-4-sulfonic acid isobornyl ester
sodium ethanolate
dl-camphene
B
1,7,7-trimethyl bicyclo[2.2.1]heptan-2-ol
1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one
A
d-borneol
B
1,7,7-trimethyl bicyclo[2.2.1]heptan-2-ol
Conditions | Yield |
---|---|
With acetic acid; platinum Hydrogenation; | |
With copper at 120 - 150℃; under 7600 - 69920 Torr; Hydrogenation; |
exo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol formate
rac-endo-borneol
B
1,7,7-trimethyl bicyclo[2.2.1]heptan-2-ol
Conditions | Yield |
---|---|
beim Verseifen; formic acid isobornyl ester; |
Conditions | Yield |
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at 50℃; |
Conditions | Yield |
---|---|
With hydrogen; nickel | |
With alcoholic alkali | |
With alkali metal | |
With hydrogen; copper | |
With diethyl ether; sodium Zersetzen des Reaktionsprodukts durch Wasser; |
Molecular Formula: C10H18O
Molar mass: 154.25 g/mol
EINECS: 207-353-1
Density: 0.992 g/cm3
Flash Point: 65.6 °C
Index of Refraction: 1.502
Boiling Point: 212 °C at 760 mmHg
Vapour Pressure: 0.0398 mmHg at 25°C
Melting point: 206-209 °C
Water solubility: Insoluble
Appearance: A white colored lump-solid
Product categories: Bicyclic Monoterpenes ; Alcohols ; Oxygen Compounds ; Terpenes ; Biochemistry
Structure of Borneol (CAS NO.507-70-0) :
XLogP3-AA: 2.7
H-Bond Donor: 1
H-Bond Acceptor: 1
IUPAC Name: (1R,4R,6R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-6-ol
Canonical SMILES: CC1(C2CCC1(C(C2)O)C)C
Isomeric SMILES: C[C@@]12CC[C@@H](C1(C)C)C[C@H]2O
InChI: InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,
8-,10+/m1/s1
InChIKey: DTGKSKDOIYIVQL-MRTMQBJTSA-N
Borneol (CAS NO.507-70-0) is used in traditional Chinese medicine as moxa. An early description can be found in the Bencao Gangmu.Isoborneol is its exo isomer.Derivatives of isoborneol are used as chiral ligands in asymmetric synthesis.
Borneol (CAS NO.507-70-0) is easily oxidized to the ketone yielding camphor. Borneol can be synthesized by reduction of camphor by the Meerwein-Ponndorf-Verley Reduction. The same reduction but then fast and irreversible with Sodium borohydride gives isoborneol as the kinetically controlled reaction product.
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | oral | 1059mg/kg (1059mg/kg) | Shika Gakuho. Journal of Dentistry. Vol. 75, Pg. 934, 1975. | |
rabbit | LDLo | oral | 2gm/kg (2000mg/kg) | Reviews of Environmental Contamination and Toxicology. Vol. 113, Pg. 47, 1990. | |
rat | LD50 | oral | 500mg/kg (500mg/kg) | French Demande Patent Document. Vol. #2448856, |
Hazard Codes: F;
Xi,Xn
Risk Statements: 11-43-22
R11:Highly flammable.
R43:May cause sensitization by skin contact.
R22:Harmful if swallowed.
Safety Statements: 16-36/37
S16:Keep away from sources of ignition.
S36/37:Wear suitable protective clothing and gloves.
RIDADR: UN 1312 4.1/PG 3
WGK Germany: 2
RTECS: DT5095000
HazardClass: 4.1
PackingGroup: III
Borneol (CAS NO.507-70-0) also can be called for Baros camphor ; 2-Borneol ; Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, (1R,2S,4R)-rel- ; 1R-endo)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol .It is a bicyclic organic compound and a terpene. The hydroxyl group in this compound is placed in an endo position.Borneol exists as two enantiomers, found in several species of Artemisia and Dipterocarpaceae, which have two different CAS numbers.And it is hazardous,so the first aid measures and others should be known.Such as: When on the skin: first,should flush skin with plenty of water immediatelyfor at least 15 minutes while removing contaminated clothing. Secondly,Get shoesmedical aid . Or in the eyes: Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids.Then get medical aid soon.While ,it's Inhaled: Remove from exposure and move to fresh air immediately.Give artificial respiration while not breathing. When breathing is difficult, give oxygen.And as soon as to get medical aid.Then you have the ingesting of the product : Wash mouth out with water,and get medical aid immediately.Notes to physician: Treat supportively and symptomatically. In addition, Borneol (CAS NO.507-70-0) can be stable under normal temperature and pressure conditions.It is not compatible with strong oxidizing agents, ignition sources, and you must not take it with incompatible materials.And also prevent it to broken down into hazardous decomposition products: carbon dioxide,carbon monoxide.