(1R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione | CAS No. 10334-26-6

(1R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione

Basic Information

CAS Number

10334-26-6

Molecular Formula

C10H14O2

Molecular Weight

166.22 g/mol

AD

Basic Physical Properties

Melting Point

200-203 °C

Boiling Point

254.44°C (rough estimate)

Flash Point

83.0±4.4 °C

Refractive Index

1.5200 (estimate)

Vapor Pressure

0.1±0.4 mmHg at 25°C

Specific Rotation

-101° (20/D)(c=2, C6H5CH3)

CC1(C2CCC1(C(=O)C2=O)C)C

InChI

InChI=1S/C10H14O2/c1-9(2)6-4-5-10(9,3)8(12)7(6)11/h6H,4-5H2,1-3H3/t6-,10+/m1/s1

InChIKey

VNQXSTWCDUXYEZ-LDWIPMOCSA-N

LogP

1.5806999999999998

Topological Polar Surface Area

34.14 Ų

Hydrogen Bond Donor/Acceptor

0 / 2

Complexity

278

Safety Information

View Safety Information

GHS Hazard Pictograms

H317H317

Hazard Statement

H317 May cause an allergic skin reaction
Sensitization, Skin

Synonyms & References

English

  • D-camphorquinone
  • VNQXSTWCDUXYEZ-LDWIPMOCSA-N
  • EINECS 207-363-6
  • 2,3-BORNANEDIONE, (+/-)-
  • MFCD00082863
  • (1R)-bornane-2,3-dione
  • NSC-285
  • SCHEMBL2245538
  • 10334-26-6
  • J-520205
  • (1R,4S)-1,7,7-trimethylnorbornane-2,3-dione
  • (1R)-(-)-Camphorquinone
  • 2,3-bornanedione;DL-Camphorquinone
  • EINECS 233-814-1
  • RAL3591W33
  • D-CAMPHORCHINONE
  • (1R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione
  • CCRIS 6299
  • Camphorquinone, 97%
  • dl-Bornane-2,3-dione
  • Q27116959
  • LMPR0102120034
  • BICYCLO(2.2.1)HEPTANE-2,3-DIONE, 1,7,7-TRIMETHYL-, (+/-)-
  • (1R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione
  • (1R)-(-)-Camphorquinone, 99%
  • UNII-RAL3591W33
  • DL-BORNANE-2,3-DION
  • AS-69585
  • CS-0179388
  • (1R,4S)-1,7,7-trimethyl-bicyclo[2.2.1]heptane-2,3-dione
  • D97678

MDL Number

MFCD00082863

Customs Code

2914299000

FAQ

What regulatory guidelines apply to (1R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione (CAS: 10334-26-6)?

The compound (1R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione (CAS: 10334-26-6) falls under the scope of the Globally Harmonized System of Classification and Labelling of Chemicals (GHS). It may also be regulated under the European Union's Registration, Evaluation, Authorization and Restriction of Chemicals (REACH) regulation. For U.S. based regulations, the U.S. Food and Drug Administration (FDA) and Environmental Protection Agency (EPA) have specific requirements for handling and reporting of chemical substances.

Are there alternatives to (1R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione (CAS: 10334-26-6) in synthesis?

There are several alternatives to (1R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione (CAS: 10334-26-6) in synthetic chemistry. Common alternatives include other diones, cyclic ketones, and various cyclic compounds that can serve similar functional groups or structural analogs. Isomers and structural analogs such as (1S,4R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione and related dioxanes are often used as alternatives.

What is the market or research trend for (1R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione (CAS: 10334-26-6)?

The research and market trends for (1R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione (CAS: 10334-26-6) indicate increasing interest in its application in medicinal chemistry and material science. Recent studies focus on its potential as a precursor in drug synthesis and as a building block for polymers. The market is seeing growth due to its unique properties, such as stability and reactivity, which make it valuable in various academic and industrial settings.

How should waste containing (1R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione (CAS: 10334-26-6) be handled?

Handling waste containing (1R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione (CAS: 10334-26-6) requires careful consideration of environmental and safety regulations. Waste should be collected in appropriate containers and labeled with the correct chemical name and CAS number. For safe disposal, it is recommended to use professional waste disposal services. Incineration can be an effective method, provided it is conducted in an environmentally compliant facility. Additionally, any potential hazardous materials should be neutralized or treated before disposal to prevent environmental contamination.

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