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100313-48-2

5,6-Dihydro-2H-pyran-3-carboxylic acid, a derivative of pyran with a molecular formula C6H8O3, is a six-membered heterocyclic compound that contains one oxygen atom in its ring. This versatile molecule is known for its ability to participate in various chemical reactions, making it a valuable intermediate in the synthesis of pharmaceuticals and organic compounds. It also serves as a building block for the preparation of other pyran derivatives and related compounds, showcasing its potential in the development of new drugs and therapeutic agents.

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  • 100313-48-2 Structure

  • Basic information

    1. Product Name: 5,6-DIHYDRO-2H-PYRAN-3-CARBOXYLIC ACID
    2. Synonyms: 5,6-DIHYDRO-2H-PYRAN-3-CARBOXYLIC ACID
    3. CAS NO:100313-48-2
    4. Molecular Formula: C6H8O3
    5. Molecular Weight: 128.13
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100313-48-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 275℃
    3. Flash Point: 121℃
    4. Appearance: /
    5. Density: 1.268
    6. Vapor Pressure: 0.00144mmHg at 25°C
    7. Refractive Index: 1.513
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 5,6-DIHYDRO-2H-PYRAN-3-CARBOXYLIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5,6-DIHYDRO-2H-PYRAN-3-CARBOXYLIC ACID(100313-48-2)
    12. EPA Substance Registry System: 5,6-DIHYDRO-2H-PYRAN-3-CARBOXYLIC ACID(100313-48-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 100313-48-2(Hazardous Substances Data)

100313-48-2 Usage

Uses

Used in Pharmaceutical Industry:
5,6-Dihydro-2H-pyran-3-carboxylic acid is used as an intermediate in the synthesis of various pharmaceuticals for its ability to undergo multiple chemical reactions, contributing to the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 5,6-Dihydro-2H-pyran-3-carboxylic acid is utilized as a building block for the preparation of other pyran derivatives and related compounds, highlighting its versatility and importance in creating a wide range of organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 100313-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,1 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 100313-48:
(8*1)+(7*0)+(6*0)+(5*3)+(4*1)+(3*3)+(2*4)+(1*8)=52
52 % 10 = 2
So 100313-48-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O3/c7-6(8)5-2-1-3-9-4-5/h2H,1,3-4H2,(H,7,8)

100313-48-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-Dihydro-2H-pyran-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3,6-dihydro-2H-pyran-5-carboxylic acid

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:100313-48-2 SDS

100313-48-2Relevant articles and documents

The enantioselective hydrogenation of 5,6-dihydro-2H-pyran-3-carboxylic acid over a cinchona alkaloid-modified palladium catalyst: Asymmetric synthesis of a cockroach attractant

Szori, Kornel,Szollosi, Gyoergy,Bartok, Mihaly

, p. 1354 - 1358 (2008)

A novel application of a cinchona-modified supported Pd catalyst is presented. The key step in the asymmetric synthesis of the cockroach attractant methyl (+)-tetrahydro-2H-pyran-3-carboxylate was the enantioselective hydrogenation of 5,6-dihydro-2H-pyran

Iridium-catalyzed enantioselective hydrogenation of unsaturated heterocyclic acids

Song, Song,Zhu, Shou-Fei,Pu, Liu-Yang,Zhou, Qi-Lin

supporting information, p. 6072 - 6075 (2013/07/05)

Spiral binding: A highly enantioselective hydrogenation of unsaturated heterocyclic acids has been developed by using chiral iridium/spirophosphino oxazoline catalysts (see scheme; BArF-=tetrakis[3,5- bis(trifluoromethyl)phenyl]borate, Boc=tert-butoxycarbonyl). This reaction provided an efficient method for the preparation of optically active heterocyclic acids with excellent enantioselectivities. Copyright

Derivatives of 5,6-Dihydro-2H-pyran-3-carboxylic acid

Spreitzer, Helmut,Mueller, Petra,Buchbauer, Gerhard

, p. 963 - 970 (2007/10/02)

Some derivatives of 5,6-dihydro-2H-pyran-3-carboxaldehyde (7) and of its oxidation product 5,6-dihydro-2H-pyran-3-carboxylic acid (8) have been prepared.The aldehyde derivatives as well as the amides and esters of 8 have been tested in an insecticidal/fun

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