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2H-1-Benzothiopyran, 3,4-dihydro-4-methyl-, also known as 4-methyl-3,4-dihydro-2H-1-benzothiopyran, is an organic compound with the chemical formula C10H10OS. It is a heterocyclic compound consisting of a benzene ring fused to a thiopyran ring, with a methyl group attached to the 4-position. 2H-1-Benzothiopyran, 3,4-dihydro-4-methyl- is a colorless to pale yellow liquid with a molecular weight of 178.25 g/mol. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain antifungal agents. Due to its potential applications in the chemical industry, it is important to understand its properties and reactivity.

6110-00-5

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6110-00-5 Usage

Chemical class

Benzene and substituted derivatives

Physical state

Colorless to pale yellow liquid

Odor

Sweet, fruity

Main uses

Manufacture of fragrances and flavorings, production of other organic compounds

Potential pharmacological properties

Studied as a potential anti-inflammatory agent

Caution

Use and handle with care to avoid health and environmental risks

Check Digit Verification of cas no

The CAS Registry Mumber 6110-00-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,1 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6110-00:
(6*6)+(5*1)+(4*1)+(3*0)+(2*0)+(1*0)=45
45 % 10 = 5
So 6110-00-5 is a valid CAS Registry Number.

6110-00-5Upstream product

6110-00-5Downstream Products

6110-00-5Relevant academic research and scientific papers

MECHANISM OF THE THIO-CLAISEN REARRANGEMENT OF 3-METHYLALLYL PHENYL SULFIDE

Danilova, T. A.,Aukharieva, R. G.,Petrov, S. N.,Grobovenko, S. Ya.,Viktorova, E. A.

, p. 883 - 886 (1981)

The thio-Claisen rearrangement of isomeric 3- and 1-methylallyl phenyl sulfides was investigated.It is demonstrated that the thio-Claisen rearrangement of the 3-methyl isomer is preceded by its thioallyl rearrangement to the 1-methyl isomer.The latter undergoes thio-Claisen rearrangement to o-(3-methylallyl)thiophenol, which is cyclized to 2-ethyl-2,3-dihydrobenzothiophene and 2-methylthiochroman under the reaction conditions.

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