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PYRAN-3-CARBONITRILE, TETRAHYDRO-, with the molecular formula C6H7NO, is a white solid chemical compound known for its versatility in various industrial applications. It serves as a crucial intermediate in the synthesis of a wide range of pharmaceuticals, agrochemicals, and other organic compounds, highlighting its importance in the development of antiviral, anti-inflammatory, and other therapeutic agents.

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  • 89464-26-6 Structure
  • Basic information

    1. Product Name: PYRAN-3-CARBONITRILE, TETRAHYDRO-
    2. Synonyms: PYRAN-3-CARBONITRILE, TETRAHYDRO-;tetrahydro-2H-pyran-3-carbonitrile
    3. CAS NO:89464-26-6
    4. Molecular Formula: C6H9NO
    5. Molecular Weight: 111.14176
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89464-26-6.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: PYRAN-3-CARBONITRILE, TETRAHYDRO-(CAS DataBase Reference)
    10. NIST Chemistry Reference: PYRAN-3-CARBONITRILE, TETRAHYDRO-(89464-26-6)
    11. EPA Substance Registry System: PYRAN-3-CARBONITRILE, TETRAHYDRO-(89464-26-6)
  • 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: 89464-26-6(Hazardous Substances Data)

89464-26-6 Usage

Uses

Used in Pharmaceutical Industry:
PYRAN-3-CARBONITRILE, TETRAHYDROis used as a key intermediate in the synthesis of various drugs and compounds for the treatment of different medical conditions. Its role in creating antiviral and anti-inflammatory medications makes it an essential component in the development of therapeutic agents.
Used in Agrochemical Production:
In the agrochemical industry, PYRAN-3-CARBONITRILE, TETRAHYDROis utilized as a building block for the production of various agrochemicals, contributing to the development of effective solutions for agricultural applications.
Used in Specialty Chemicals Manufacturing:
PYRAN-3-CARBONITRILE, TETRAHYDROis also employed in the manufacturing of dyes, pigments, and other specialty chemicals, showcasing its diverse applications across different industries. Its involvement in these processes highlights its importance in creating a broad spectrum of products with specific color and functional properties.

Check Digit Verification of cas no

The CAS Registry Mumber 89464-26-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,4,6 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89464-26:
(7*8)+(6*9)+(5*4)+(4*6)+(3*4)+(2*2)+(1*6)=176
176 % 10 = 6
So 89464-26-6 is a valid CAS Registry Number.

89464-26-6SDS

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 oxane-3-carbonitrile

1.2 Other means of identification

Product number -
Other names Tetrahydro-Pyran-3-Carbonitrile

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:89464-26-6 SDS

89464-26-6Relevant articles and documents

N-methyl-N-phenyl-5-oxa-1-azaspiro[2.5]oct-1-en-2-amine - Synthesis and reactions of a synthon for AN UNKNOWN α-AMINO ACID

Loepfe, Michael,Linden, Anthony,Heimgartner, Heinz

, p. 1267 - 1282 (2011/05/14)

The synthesis of the heterospirocyclic amino azirine N-methyl-N-phenyl-5- oxa-1-azaspiro[2.5]oct-1-en-2-amine (6a) was achieved from 3,4-dihydro-2H-pyrane (7) via N-methyl-N-phenyltetrahydropyran-3-thiocarboxamide (11). The reactions of 6a with thiobenzoic acid and Z-Phe-OH, respectively, leading to the corresponding 3-benzoylaminotetrahydropyran-3-thiocarboxamide (13) and the diastereoisomeric dipeptide amides (14), respectively, demonstrate that 6a is a valuable synthon for the hitherto unknown 3-aminotetrahydropyrane-3-carboxylic acid. The structure of 13 was established by X-Ray crystallography. The Japan Institute of Heterocyclic Chemistry.

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