Camphor

Base Information

  • PRODUCT:Camphor
  • CAS.:76-22-2
  • MF:C10H16O
  • Molecular Weight:152.236
  • Purity:99%

Product Details

CAS： 76-22-2

MF： C10H16O

Appearance： Colourless solid

Factory Supply Hot Sale Camphor 76-22-2 Reasonable Price

  • Molecular Formula:C10H16O
  • Molecular Weight:152.236
  • Appearance/Colour:Colourless solid 
  • Melting Point:179 °C 
  • Boiling Point:207.4 °C at 760 mmHg 
  • Flash Point:64.4 °C 
  • PSA：17.07000 
  • Density:0.982 g/cm3 
  • LogP:2.40170 
  • IDLH: 200 mg/m3See: 76222  
  • IDLH:1395 
  • IDLH:140 
  • IDLH:2230 

2-Bornanone(Cas 76-22-2) Usage

Who Evaluation

Evaluation year: 2004

EXPOSURE ROUTES

inhalation, skin absorption, ingestion, skin and/or eye contact

FIRST AID

(See procedures) Eye:Irrigate immediately Skin:Soap wash immediately Breathing:Respiratory support Swallow:Medical attention immediately

Consumer Uses

ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.

InChI:InChI=1/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3

76-22-2 Relevant articles

Rapid, chemoselective and mild oxidation protocol for alcohols and ethers with recyclable N-chloro-N-(phenylsulfonyl)benzenesulfonamide

Badani, Purav,Chaturbhuj, Ganesh,Ganwir, Prerna,Misal, Balu,Palav, Amey

supporting information, (2021/06/03)

Chlorine is the 20th most abundant eleme...

carba Nicotinamide Adenine Dinucleotide Phosphate: Robust Cofactor for Redox Biocatalysis

D?ring, Manuel,Sieber, Volker,Simon, Robert C.,Tafertshofer, Georg,Zachos, Ioannis

supporting information, p. 14701 - 14706 (2021/05/13)

Here we report a new robust nicotinamide...

Aerobic oxidation of alcohols catalyzed by in situ generated gold nanoparticles inside the channels of periodic mesoporous organosilica with ionic liquid framework

Bigdeli, Akram,Karimi, Babak,Khodadadi Karimvand, Somaiyeh,Khorasani, Mojtaba,Safari, Ali Asghar,Vali, Hojatollah

supporting information, p. 70 - 79 (2020/06/08)

In situ generated gold nanoparticles ins...

Method for hydrogenolysis of halides

-

Paragraph 0232; 0269-0271, (2021/01/11)

The invention discloses a method for hyd...

76-22-2 Process route

(+/-)-fenchone
18492-37-0,126-21-6

(+/-)-fenchone

m-cymene
535-77-3

m-cymene

1,2-dimethyl-4-ethylbenzene
934-80-5

1,2-dimethyl-4-ethylbenzene

Camphor
76-22-2,68546-28-1

Camphor

Conditions
Conditions Yield
aluminum oxide; at 299.9 - 404.9 ℃; Rate constant; Kinetics; Thermodynamic data; reactions over var. alumina catalists at sev. temperatures, ΔH(excit), ΔS(excit), ΔG(excit);
1,7,7-trimethyl bicyclo[2.2.1]heptan-2-ol
507-70-0

1,7,7-trimethyl bicyclo[2.2.1]heptan-2-ol

dl-camphene
565-00-4

dl-camphene

Camphor
76-22-2,68546-28-1

Camphor

Conditions
Conditions Yield
With copper; at 135 - 140 ℃;

76-22-2 Upstream products

  • 110-86-1
    110-86-1

    pyridine

  • 52162-25-1
    52162-25-1

    bornan-2-one-diethylacetal

  • 75-36-5
    75-36-5

    acetyl chloride

  • 56-23-5
    56-23-5

    tetrachloromethane

76-22-2 Downstream products

  • 67396-44-5
    67396-44-5

    p-Anisylisoborneol

  • 251576-26-8
    251576-26-8

    C10H19N

  • 1449691-93-3
    1449691-93-3

    5-(4-chloro-3-methylphenyl)-1-[(4-methylphenyl)methyl]-N-[(1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]-1H-pyrazole-3-carboxamide

  • 84731-76-0
    84731-76-0

    1,7,7-trimethyl-2-pyridin-2-yl-bicyclo[2.2.1]heptan-2-ol

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