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1-(Biphenyl-4-yl)-2-[(2,6-dimethyl-2H-pyran-4-yl)sulfanyl]ethanone is a complex organic compound with the molecular formula C20H20O2S. It is characterized by a biphenyl group attached to a carbonyl group, which is further connected to a sulfanyl group. The sulfanyl group is part of a 2,6-dimethyl-2H-pyran-4-yl ring, which contributes to the compound's unique structure and properties. This chemical is not commonly found in household products or foods, and its applications are typically limited to specialized industrial or research settings. Due to its specific structure, it may have unique chemical reactivity or be used in the synthesis of other compounds. However, without further context or specific use cases, it's challenging to provide a more detailed summary of its applications or properties.

6275-20-3

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6275-20-3 Usage

Molecular Weight

324.44 g/mol

Biphenyl-4-yl group

An aromatic hydrocarbon consisting of two fused benzene rings, with the functional group attached to the fourth carbon of the first benzene ring.

2-[(2,6-dimethyl-2H-pyran-4-yl)sulfanyl]ethanone group

Contains a pyran ring (a six-membered oxygen-containing ring) with two methyl groups at the 2nd and 6th positions, a sulfur atom connected to the 4th carbon of the pyran ring, and a ketone group (C=O) attached to the 2nd carbon of the ethanone chain.

Functional Groups

Aromatic hydrocarbon (biphenyl-4-yl)
Pyran ring (2,6-dimethyl-2H-pyran-4-yl)
Sulfanyl group (-S-)
Ketone group (C=O)

Organic synthesis

As a building block for creating more complex organic molecules.

Pharmaceutical research

Potential use as a drug intermediate.

Chemical reagent

Due to its unique molecular structure and potential reactivity.

Industrial Applications

May have other industrial applications due to its unique molecular structure and potential reactivity.

Solubility

The solubility of DMPK is not explicitly mentioned in the material provided, but it is likely to be soluble in organic solvents such as ethanol, methanol, or acetone, given its nonpolar nature.

Stability

The stability of DMPK is not explicitly mentioned in the material provided, but it is expected to be stable under normal laboratory conditions, as it is a common building block in organic synthesis and pharmaceutical research.

Reactivity

The reactivity of DMPK is not explicitly mentioned in the material provided, but its unique molecular structure suggests that it may have potential reactivity with various reagents, making it useful in organic synthesis and pharmaceutical research.

Safety

The safety information for DMPK is not provided in the material, but as with any chemical compound, it is essential to follow proper safety protocols, including wearing appropriate personal protective equipment (PPE) and handling the compound in a well-ventilated area or fume hood.

Check Digit Verification of cas no

The CAS Registry Mumber 6275-20-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6275-20:
(6*6)+(5*2)+(4*7)+(3*5)+(2*2)+(1*0)=93
93 % 10 = 3
So 6275-20-3 is a valid CAS Registry Number.

6275-20-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,6-dimethylpyrylium-4-yl)sulfanyl-1-(4-phenylphenyl)ethanone,bromide

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:6275-20-3 SDS

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