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612481-34-2

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612481-34-2 Usage

Chemical Class

Naphthols

Substructure

Naphthalene

Biological Activities

Known for its biological activities

Natural Sources

Can be found in various natural sources

Applications

Potential applications in medicine, pharmaceuticals, and organic chemistry

Chemical Structure

Complex and long name, with stereochemistry specified as (1S,4R,4aS,5R,8aR)-(9CI)

Research and Development

Interesting target for further research and development in the scientific community

Molecular Weight

Approximately 230.3 g/mol (calculated from the molecular formula)

Physical State

Likely a solid at room temperature (based on the presence of multiple rings and the complexity of the structure)

Melting Point

Not provided, but can be determined experimentally

Boiling Point

Not provided, but can be determined experimentally

Optical Activity

Exhibits optical activity due to the presence of chiral centers (1S,4R,4aS,5R,8aR)-(9CI)

Stability

Stability can be assessed through experimental methods, but the presence of multiple rings and a hydroxyl group suggests it may be relatively stable under certain conditions

Reactivity

May react with various reagents due to the presence of a hydroxyl group and other functional groups in the structure

Synthesis

Can be synthesized through various chemical reactions, potentially involving the manipulation of naphthalene or related compounds

Derivatives

May have various derivatives with different functional groups or modifications to the structure, which could exhibit different properties and applications

Toxicity

Not provided, but should be assessed through experimental methods as it has potential applications in medicine and pharmaceuticals

Environmental Impact

Not provided, but should be considered when evaluating the use and disposal of this compound, especially in the context of pharmaceuticals and organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 612481-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,2,4,8 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 612481-34:
(8*6)+(7*1)+(6*2)+(5*4)+(4*8)+(3*1)+(2*3)+(1*4)=132
132 % 10 = 2
So 612481-34-2 is a valid CAS Registry Number.

612481-34-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,4R,4aS,5R,8aR)-8-Methylene-1,4,4a,5,6,7,8,8a-octahydro-1,4-methano-naphthalen-5-ol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:612481-34-2 SDS

612481-34-2Downstream Products

612481-34-2Relevant articles and documents

Enantioselective total syntheses of (+)- and (-)-ottelione A and (+)- and (-)-ottelione B. Absolute configuration of the novel, biologically active natural products

Mehta, Goverdhan,Islam, Kabirul

, p. 6733 - 6736 (2007/10/03)

Following our recent total synthesis of the biologically potent natural products otteliones A and B in racemic form, we have now accomplished the total synthesis of both the enantiomers of otteliones A and B through an enantiodivergent strategy emanating from the readily available Diels-Alder adduct of cyclopentadiene and p-benzoquinone. These endeavors have led to the elucidation of the absolute configuration of naturally occurring otteliones A and B.

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