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69316-10-5

3-(5-CHLORO-2-METHOXY-PHENYL)-3-OXO-PROPIONITRILE is a chemical compound with the molecular formula C10H8ClNO3. It is a yellow crystalline powder that is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 3-(5-CHLORO-2-METHOXY-PHENYL)-3-OXO-PROPIONITRILE is also known for its potential as an antibacterial agent and has been studied for its antimicrobial properties. It is important to handle this chemical with care, as it may be harmful if ingested or inhaled, and can cause skin and eye irritation. Additionally, it should be stored in a cool, dry place away from incompatible materials.

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  • 69316-10-5 Structure

  • Basic information

    1. Product Name: 3-(5-CHLORO-2-METHOXY-PHENYL)-3-OXO-PROPIONITRILE
    2. Synonyms: 3-(5-CHLORO-2-METHOXY-PHENYL)-3-OXO-PROPIONITRILE;5-Chloro-2-methoxy-b-oxo-benzenepropanenitrile
    3. CAS NO:69316-10-5
    4. Molecular Formula: C10H8ClNO2
    5. Molecular Weight: 209.63
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69316-10-5.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: 3-(5-CHLORO-2-METHOXY-PHENYL)-3-OXO-PROPIONITRILE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(5-CHLORO-2-METHOXY-PHENYL)-3-OXO-PROPIONITRILE(69316-10-5)
    11. EPA Substance Registry System: 3-(5-CHLORO-2-METHOXY-PHENYL)-3-OXO-PROPIONITRILE(69316-10-5)

  • 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: 69316-10-5(Hazardous Substances Data)

69316-10-5 Usage

Uses

Used in Pharmaceutical Industry:
3-(5-CHLORO-2-METHOXY-PHENYL)-3-OXO-PROPIONITRILE is used as an intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a key component in the development of new drugs and medications.
Used in Agrochemical Industry:
3-(5-CHLORO-2-METHOXY-PHENYL)-3-OXO-PROPIONITRILE is also used as an intermediate in the synthesis of agrochemicals. Its potential applications in this industry include the development of new pesticides and herbicides to improve crop yields and protect against pests.
Used as an Antibacterial Agent:
3-(5-CHLORO-2-METHOXY-PHENYL)-3-OXO-PROPIONITRILE has been studied for its antimicrobial properties and is used as a potential antibacterial agent. Its ability to inhibit the growth of bacteria makes it a valuable compound in the development of new antibiotics and antimicrobial treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 69316-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,1 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69316-10:
(7*6)+(6*9)+(5*3)+(4*1)+(3*6)+(2*1)+(1*0)=135
135 % 10 = 5
So 69316-10-5 is a valid CAS Registry Number.

69316-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(5-Chloro-2-methoxyphenyl)-3-oxopropanenitrile

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:69316-10-5 SDS

69316-10-5Relevant articles and documents

3-Substituted-(5-arylfuran-2-ylcarbonyl)guanidines as NHE-1 inhibitors

Lee, Sunkyung,Kim, Taemi,Lee, Byung Ho,Yoo, Sung-eun,Lee, Kyunghee,Yi, Kyu Yang

, p. 1291 - 1295 (2008/02/02)

The C-3 substituents effect on NHE-1 inhibitory activity of (5-arylfuran-2-ylcarbonyl)guanidines, previously identified as potent NHE-1 inhibitors, was investigated. The introduction of amine or alkyl groups at the 3-position of the furan ring, next to the acylguanidine moiety, remarkably improves NHE-1 inhibitory potency. Especially the important finding is that 5-(2,5-dichloro)phenyl and 5-(2-methoxy-5-chloro)phenyl derivatives exhibit high NHE-1 inhibitory activities (IC50 0.02 μM) that match those of 3-unsubstituted derivatives.

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