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188481-45-0

(R)-A-HYDROXY-3-FURANACETONITRILE, with the molecular formula C6H5NO2, is a colorless liquid characterized by a faint, sweet odor. It is a chemical compound that serves as a crucial intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. Its versatility as a building block in organic synthesis and its role in the production of chiral compounds make it an indispensable tool in the development of new chemical entities for a range of industries.

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  • 188481-45-0 Structure

  • Basic information

    1. Product Name: (R)-A-HYDROXY-3-FURANACETONITRILE
    2. Synonyms: (R)-A-HYDROXY-3-FURANACETONITRILE
    3. CAS NO:188481-45-0
    4. Molecular Formula: C6H5NO2
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 188481-45-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (R)-A-HYDROXY-3-FURANACETONITRILE(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-A-HYDROXY-3-FURANACETONITRILE(188481-45-0)
    11. EPA Substance Registry System: (R)-A-HYDROXY-3-FURANACETONITRILE(188481-45-0)

  • 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: 188481-45-0(Hazardous Substances Data)

188481-45-0 Usage

Uses

Used in Pharmaceutical Industry:
(R)-A-HYDROXY-3-FURANACETONITRILE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties. Its role in the production of chiral compounds is particularly valuable, as chirality is a critical factor in the efficacy and safety of many medications.
Used in Agrochemical Industry:
In the agrochemical sector, (R)-A-HYDROXY-3-FURANACETONITRILE is utilized as an intermediate in the creation of agrochemicals, such as pesticides and herbicides. Its involvement in the synthesis process helps in designing more effective and targeted agrochemicals to improve crop protection and yield.
Used as a Reagent in Organic Chemical Reactions:
(R)-A-HYDROXY-3-FURANACETONITRILE also serves as a reagent in various organic chemical reactions, facilitating the formation of desired products and enhancing the efficiency of synthesis processes. Its application in this area underscores its importance in the broader field of organic chemistry.
Overall, (R)-A-HYDROXY-3-FURANACETONITRILE's multifaceted applications across different industries highlight its significance as a versatile and valuable chemical compound in modern science and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 188481-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,4,8 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 188481-45:
(8*1)+(7*8)+(6*8)+(5*4)+(4*8)+(3*1)+(2*4)+(1*5)=180
180 % 10 = 0
So 188481-45-0 is a valid CAS Registry Number.

188481-45-0SDS

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 (R)-2-(furan-3-yl)-2-hydroxyacetonitrile

1.2 Other means of identification

Product number -
Other names (R)-A-Hydroxy-3-Furanacetonitrile

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:188481-45-0 SDS

188481-45-0Downstream Products

188481-45-0Relevant articles and documents

Stereoselective synthesis of thienyl and furyl analogues of ephedrine

Effenberger, Franz,Eichhorn, Joachim

, p. 469 - 476 (2007/10/03)

The stereoselective syntheses of thienyl and furyl analogues of ephedrine starting from (R)- and (S)-cyanohydrins, respectively, are described. Addition of methyl Grignard to the O-trimethylsilyl protected optically active cyanohydrins (R)- and (S)-3 and hydrogenation of the resulting imino intermediates gives the erythro-2-amino alcohols 4 with high diastereoselectivity. Their reductive methylation leads to the enantiomerically pure thiophene analogues (1S,2S)- and (1R,2R)-6a, (1R,2S)- and (1S,2R)-6b as well as to the furan analogues (1S,2S)-6c and (1R,2S)-6d of ephedrine, The biological activity of the new compounds is under investigation.

Ueber die erste rekombinante Hydroxynitril-Lyase und ihre Anwendung in der Synthese von (S)-Cyanhydrinen

Foerster, Siegfried,Roos, Juergen,Effenberger, Franz,Wajant, Harald,Sprauer, Achim

, p. 493 - 494 (2007/10/03)

Keywords: Asymmetrische Synthesen; (S)-Cyanhydrine; Enzymkatalyse; Lyasen

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