84194-91-2

Basic information

• Product Name: (1R,2S)-2-CHLORO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-OL
• Synonyms: (1R,2S)-2-CHLORO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-OL
• CAS NO: 84194-91-2
• Molecular Formula: C10H11ClO
• Molecular Weight: 182.64674
• Mol File: 84194-91-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 332.1°C at 760 mmHg
• Flash Point: 154.6°C
• Appearance: /
• Density: 1.24g/cm³
• Vapor Pressure: 5.96E-05mmHg at 25°C
• Refractive Index: 1.589
• CAS DataBase Reference: (1R,2S)-2-CHLORO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-OL(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S)-2-CHLORO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-OL(84194-91-2)
• EPA Substance Registry System: (1R,2S)-2-CHLORO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-OL(84194-91-2)

Safety Data

• Hazardous Substances Data: 84194-91-2(Hazardous Substances Data)

Usage

General Description

The chemical compound "(1R,2S)-2-chloro-1,2,3,4-tetrahydro-naphthalen-1-ol" is a chiral alcohol with a chlorine atom attached to the second carbon and a hydroxyl group on the first carbon of a tetrahydronaphthalene ring. (1R,2S)-2-CHLORO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-OL is used in organic synthesis as a building block for the creation of more complex molecules. It has potential applications in the pharmaceutical industry as a starting material for the synthesis of various drugs and biologically active compounds. The stereochemistry of this compound is important as it can influence its reactivity and selectivity in chemical reactions. Overall, "(1R,2S)-2-chloro-1,2,3,4-tetrahydro-naphthalen-1-ol" is a versatile compound with a range of potential uses in medicinal chemistry and organic synthesis.

InChI:InChI=1/C10H11ClO/c11-9-6-5-7-3-1-2-4-8(7)10(9)12/h1-4,9-10,12H,5-6H2/t9-,10+/m0/s1

Upstream product

• 447-53-0 1,2-Dihydronaphthalene 
• 17215-80-4 2-chloro-1-tetralone 

Relevant articles and documents

Cross-Linked Artificial Enzyme Crystals as Heterogeneous Catalysts for Oxidation Reactions

Designing systems that merge the advantages of heterogeneous catalysis, enzymology, and molecular catalysis represents the next major goal for sustainable chemistry. Cross-linked enzyme crystals display most of these essential assets (well-designed mesoporous support, protein selectivity, and molecular recognition of substrates). Nevertheless, a lack of reaction diversity, particularly in the field of oxidation, remains a constraint for their increased use in the field. Here, thanks to the design of cross-linked artificial nonheme iron oxygenase crystals, we filled this gap by developing biobased heterogeneous catalysts capable of oxidizing carbon-carbon double bonds. First, reductive O2 activation induces selective oxidative cleavage, revealing the indestructible character of the solid catalyst (at least 30 000 turnover numbers without any loss of activity). Second, the use of 2-electron oxidants allows selective and high-efficiency hydroxychlorination with thousands of turnover numbers. This new technology by far outperforms catalysis using the inorganic complexes alone, or even the artificial enzymes in solution. The combination of easy catalyst synthesis, the improvement of "omic" technologies, and automation of protein crystallization makes this strategy a real opportunity for the future of (bio)catalysis.