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Catalog Number:
41056
CAS Number:
111795-43-8
(R)-3,3'-Dibromo-1,1'-bi-2-naphthol
Purity:
≥ 98% (Chiral purity)
Synonym(s):
(R)-3,3'-Dibromo-2,2'-dihydroxy-1,1'-binaphthyl
Documents
$380.57 /1G
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Product Information

(R)-3,3'-Dibromo-1,1'-bi-2-naphthol is a specialized compound known for its unique properties and applications in various fields, particularly in organic synthesis and materials science. This compound features two bromine atoms and hydroxyl groups that enhance its reactivity, making it an excellent candidate for use in asymmetric synthesis and catalysis. Its chirality allows for the production of enantiomerically pure compounds, which is crucial in pharmaceutical applications where the efficacy of drugs can depend on their stereochemistry.

In addition to its role in synthesis, (R)-3,3'-Dibromo-1,1'-bi-2-naphthol is also utilized in the development of advanced materials, such as organic light-emitting diodes (OLEDs) and liquid crystal displays (LCDs). Its ability to act as a ligand in coordination chemistry further expands its utility in creating novel compounds with tailored properties. Researchers and industry professionals can leverage this compound for innovative applications, making it a valuable addition to any chemical inventory.

Synonyms
(R)-3,3'-Dibromo-2,2'-dihydroxy-1,1'-binaphthyl
CAS Number
111795-43-8
Purity
≥ 98% (Chiral purity)
Molecular Formula
C20H12Br2O2
Molecular Weight
444.12
MDL Number
MFCD03093629
PubChem ID
10765693
Melting Point
256 - 260 °C
Appearance
White to orange to light green powder
Optical Rotation
[α]20D = 90 ± 2 ° (C = 1 in MeOH)
Conditions
Store at RT
General Information
Synonyms
(R)-3,3'-Dibromo-2,2'-dihydroxy-1,1'-binaphthyl
CAS Number
111795-43-8
Purity
≥ 98% (Chiral purity)
Molecular Formula
C20H12Br2O2
Molecular Weight
444.12
MDL Number
MFCD03093629
PubChem ID
10765693
Melting Point
256 - 260 °C
Appearance
White to orange to light green powder
Optical Rotation
[α]20D = 90 ± 2 ° (C = 1 in MeOH)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R)-3,3'-Dibromo-1,1'-bi-2-naphthol is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, allowing researchers to create complex molecules with specific properties, enhancing the efficiency of synthetic pathways.
  • Chiral Catalysis: Its unique chiral structure makes it an excellent catalyst in asymmetric synthesis, helping to produce enantiomerically pure compounds, which is crucial in pharmaceuticals.
  • Material Science: Used in the development of advanced materials, it contributes to the creation of polymers and coatings with improved thermal and mechanical properties, benefiting industries like electronics and automotive.
  • Biological Research: This compound is explored for its potential applications in medicinal chemistry, particularly in the design of new drugs targeting specific biological pathways, offering innovative solutions for health challenges.
  • Environmental Chemistry: It plays a role in the study of environmental pollutants, aiding researchers in understanding the behavior of brominated compounds in ecosystems and developing strategies for remediation.

Citations