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Benzonitrile, 2-(cyanomethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 49615-99-8 Structure
  • Basic information

    1. Product Name: Benzonitrile, 2-(cyanomethoxy)-
    2. Synonyms:
    3. CAS NO:49615-99-8
    4. Molecular Formula: C9H6N2O
    5. Molecular Weight: 158.159
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 49615-99-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzonitrile, 2-(cyanomethoxy)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzonitrile, 2-(cyanomethoxy)-(49615-99-8)
    11. EPA Substance Registry System: Benzonitrile, 2-(cyanomethoxy)-(49615-99-8)
  • 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: 49615-99-8(Hazardous Substances Data)

49615-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49615-99-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,1 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 49615-99:
(7*4)+(6*9)+(5*6)+(4*1)+(3*5)+(2*9)+(1*9)=158
158 % 10 = 8
So 49615-99-8 is a valid CAS Registry Number.

49615-99-8SDS

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 (2-cyanophenoxy)acetonitrile

1.2 Other means of identification

Product number -
Other names 2-cyanomethoxybenzonitrile

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:49615-99-8 SDS

49615-99-8Relevant articles and documents

A benzofuran-β-Alaninamide based "turn-on" fluorescent chemosensor for selective recognition of Fe3+ ions

Madhu,Sivakumar,Sribalan, Rajendran

, p. 14426 - 14434 (2019)

A benzofuran-β-Alaninamide based chemosensor, 3-(3-((4-methylbenzyl)amino)propanamido)benzofuran-2-carboxamide (BAA), was designed and synthesized for selective detection of Fe3+ ions. The binding ability of BAA towards Fe3+ in DMSO/

Syntheses of 3-acetoacetylaminobenzo[b]furan derivatives having cysteinyl leukotriene 2 receptor antagonistic activity

Ando, Kumiko,Tsuji, Eriko,Ando, Yuko,Kuwata, Noriko,Kunitomo, Jun-Ichi,Yamashita, Masayuki,Ohta, Shunsaku,Kohno, Shigekatsu,Ohishi, Yoshitaka

, p. 625 - 635 (2007/10/03)

Novel 3-acetoacetylaminobenzo[b]furan derivatives having a modified triene system at the 3-position were synthesized starting with 3-aminobenzo[b]furans. The enol isomers, 3-[(3-hydroxybul-2-enonyl)amino]benzo[b]furans (1), of the 3-acetoacetylaminobenzo[b]furans were obtained as stable isomers owing to formation of a hydrogen bonding between the enol hydroxyl group and the amidocarbonyl group. The planarity of the C-2 substituent through the C-3 side chain suggested the existence of a modified conjugational triene system in the enol compound. Cysteinyl leukotriene 1 and 2 receptor antagonistic activities for these compounds were evaluated. 2-(4-Cyanobenzoyl or ethoxycarbonyl)-3-[(2-cyano-3-hydroxybut-2-enonyl)amino]benzo[e]furans (15g, 15o, 15u) were moderately active.

Benzothiophenes and benzofurans and antiallergic use thereof

-

, (2008/06/13)

Novel benzothiophene and benzofuran derivatives having antiallergic activity are described as well as a method of manufacture, pharmaceutical compositions, and methods of use therefor. The disclosure describes the use of derivatives for prevention of the release of mediators including histamine and leukotrienes from basophils and mast cells, and prevent respiratory burst in neutrophils providing activity useful in cardiovascular disorders as well as in antiinflammatory, psoriasis, and antimigraine treatment.

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