(+)-3-Bromocamphor - ≥98%(GC) , CAS No.10293-06-8

CAS: 10293-06-8 Cat. No.: B153198 Summenformel: C₁₀H₁₅BrO Molekulargewicht: 231.13 Beilstein Registry Number: 3197240 EG-Nummer: 233-652-1

GRADE & PURITY ≥98%(GC)

Synonyms

(+)-3-Bromocamphor | BRN 3603833 | 3-BROMOCAMPHOR, (+/-)- | (+)-3-Bromocamphor, purum, >=97.0% (sum of enantiomers, GC) | 2-Bornanone, 3-bromo-, (1R,3S,4S)-(+)- | CAMPHOR, MONOBROMATED | MFCD00003744 | Bicyclo(2.2.1)heptan-2-one, 3-bromo-1,7,7-trimethyl-,

Storage

Store at 2-8°C,Protected from light,Argon charged,Desiccated

Shipped In

Wet ice

Specifications

Synonyme

(+)-3-Bromocamphor | BRN 3603833 | 3-BROMOCAMPHOR, (+/-)- | (+)-3-Bromocamphor, purum, >=97.0% (sum of enantiomers, GC) | 2-Bornanone, 3-bromo-, (1R,3S,4S)-(+)- | CAMPHOR, MONOBROMATED | MFCD00003744 | Bicyclo(2.2.1)heptan-2-one, 3-bromo-1,7,7-trimethyl-,

Spezifikationen & Reinheit

≥98%(GC)

Storage

Store at 2-8°C,Protected from light,Argon charged,Desiccated

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥98%(GC)

Namen und Kennungen

• Pubchem Sid: 504758963
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504758963
• Kanonisches Lächeln: CC1(C2CCC1(C(=O)C2Br)C)C
• IUPAC Name: (1R,3S,4S)-3-bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
• InChIKey: NJQADTYRAYFBJN-FWWHASMVSA-N
• INCHI: 1S/C10H15BrO/c1-9(2)6-4-5-10(9,3)8(12)7(6)11/h6-7H,4-5H2,1-3H3/t6-,7+,10+/m1/s1
• Isomere SMILES: C[C@@]12CC[C@@H](C1(C)C)[C@@H](C2=O)Br
• WGK Deutschland: 3
• RTECS: ED6750000
• Molekulargewicht: 231.13
• Beilstein: 3197240
• Reaxy-Rn: 2044875
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2044875&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Klasse Prenol lipids
      • Subclass Monoterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Klasse: Prenol lipids
• Subclass: Monoterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Bicyclic monoterpenoids
• Alternative Parents: Alpha-haloketones Organobromides Organic oxides Hydrocarbon derivatives Alkyl bromides
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Bicyclic monoterpenoid - Bornane monoterpenoid - Alpha-haloketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organobromide - Organohalogen compound - Carbonyl group - Alkyl halide - Alkyl bromide - Aliphatic homopolycyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in Methanol
• Empfindlichkeit: light sensitive
• Spezifische Drehung [α]: 137.5° (C=2,EtOH)
• Siedepunkt (°C): 274 °C
• Schmelzpunkt (°C): 76 °C
• Molekulargewicht: 231.130 g/mol
• XLogP3: 2.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 230.031 Da
• Monoisotopic Mass: 230.031 Da
• Topological Polar Surface Area: 17.100 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 246.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 3
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referenzen

1. Ping Li, Siyi Wang, Mengyuan Liu, Xue Dai, Huicong Shi, Weihong Zhou, Sheng Sheng, Fuan Wu.  (2024)  Antibacterial Activity and Mechanism of Three Root Exudates from Mulberry Seedlings against Ralstonia pseudosolanacearum.  Plants-Basel,  13  (4): (482).  [PMID:38498445] [10.3390/plants13040482]

Häufig gestellte Fragen

What is the purity of this product, and how is it determined?

This product is supplied at ≥98% purity, determined by gas chromatography (GC). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at 2–8 °C, protected from light, desiccated, under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

How is this product shipped?

This product ships chilled on wet ice. Unpack on arrival and transfer it to the storage condition stated above.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 10293-06-8, the molecular formula is C10H15BrO, and the molecular weight is 231.13 g/mol. InChIKey NJQADTYRAYFBJN-FWWHASMVSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.