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380636-44-2

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  • 2-Hydroxy-4-phenyl-6-methoxycarbonyl-2,3-dihydrobenzopyran (Mixture of Diastereomers)

    Cas No: 380636-44-2

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380636-44-2 Usage

Description

2-Hydroxy-4-phenyl-6-methoxycarbonyl-2,3-dihydrobenzopyran (Mixture of Diastereomers) is a complex organic compound with a unique molecular structure consisting of a benzopyran core, a hydroxyl group, a phenyl ring, and a methoxycarbonyl group. It exists as a mixture of diastereomers, which are stereoisomers that are not mirror images of each other. 2-Hydroxy-4-phenyl-6-methoxycarbonyl-2,3-dihydrobenzopyran (Mixture of Diastereomers) is characterized by its molecular formula C16H14O5 and a CAS number of 380636-44-2.

Uses

Used in Organic Synthesis:
2-Hydroxy-4-phenyl-6-methoxycarbonyl-2,3-dihydrobenzopyran (Mixture of Diastereomers) is used as a key intermediate in organic synthesis for the development of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and functional groups make it a versatile building block for the synthesis of complex organic molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Hydroxy-4-phenyl-6-methoxycarbonyl-2,3-dihydrobenzopyran (Mixture of Diastereomers) is used as a starting material or a synthetic intermediate for the preparation of drug candidates with potential therapeutic applications. Its structural features can be exploited to design and synthesize novel compounds with improved pharmacological properties, such as enhanced potency, selectivity, and bioavailability.
Used in Agrochemical Industry:
2-Hydroxy-4-phenyl-6-methoxycarbonyl-2,3-dihydrobenzopyran (Mixture of Diastereomers) also finds applications in the agrochemical industry, where it can be used as a precursor for the synthesis of bioactive compounds with pesticidal properties. These compounds can be developed into new pesticides or herbicides to control pests and diseases in agriculture, thereby increasing crop yields and ensuring food security.
Used in Specialty Chemicals Industry:
In the specialty chemicals industry, 2-Hydroxy-4-phenyl-6-methoxycarbonyl-2,3-dihydrobenzopyran (Mixture of Diastereomers) can be employed as a raw material for the production of various specialty chemicals, such as dyes, pigments, and fragrances. Its unique structural features can be utilized to create novel compounds with specific properties, such as color, stability, and sensory characteristics, which can be used in a wide range of applications, including textiles, cosmetics, and food products.

Check Digit Verification of cas no

The CAS Registry Mumber 380636-44-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,6,3 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 380636-44:
(8*3)+(7*8)+(6*0)+(5*6)+(4*3)+(3*6)+(2*4)+(1*4)=152
152 % 10 = 2
So 380636-44-2 is a valid CAS Registry Number.

380636-44-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-hydroxy-4-phenyl-3,4-dihydro-2H-chromene-6-carboxylate

1.2 Other means of identification

Product number -
Other names (4R,4S)-2-(R,S)-hydroxy-4-phenylchromane-6-carboxylic acid methyl ester

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:380636-44-2 SDS

380636-44-2Relevant articles and documents

PREPARATION PROCESS OF FESOTERODINE AND INTERMEDIATES

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Page/Page column 32, (2012/01/06)

The present invention relates to a process of synthesis of 3,3 dipheylpropylamines, which may be used as pharmaceutical intermediates in the preparation of their pharmacologically active derivatives such as fesoterodine, tolterodine, their enantiomers, pharmaceutically acceptable salts and related compounds useful as antimuscarinic agents.

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