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55745-71-6

2,3-DIHYDRO-1-BENZOFURAN-5-CARBONYL CHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 55745-71-6 Structure

  • Basic information

    1. Product Name: 2,3-DIHYDRO-1-BENZOFURAN-5-CARBONYL CHLORIDE
    2. Synonyms: BUTTPARK 36\18-17;2,3-DIHYDRO-1-BENZOFURAN-5-CARBONYL CHLORIDE;2,3-DIHYDROBENZO[B]FURAN-5-CARBONYL CHLORIDE;2,3-Dihydro-1-benzofurane-5-carbonylchloride;5-Benzofurancarbonyl chloride, 2,3-dihydro- (9CI);2,3-dihydrobenzofuran-5-carbonyl chloride
    3. CAS NO:55745-71-6
    4. Molecular Formula: C9H7ClO2
    5. Molecular Weight: 182.6
    6. EINECS: N/A
    7. Product Categories: ACIDHALIDE;Carbonyl Chlorides;Furans, Benzofurans & Dihydrobenzofurans;Furan&Benzofuran;Carbonyl Chlorides;Furans, Benzofurans & Dihydrobenzofurans
    8. Mol File: 55745-71-6.mol

  • Chemical Properties

    1. Melting Point: 49 °C
    2. Boiling Point: 145-147°C 1mm
    3. Flash Point: 110.3 °C
    4. Appearance: white to light yellow crystal powder
    5. Density: 1.342 g/cm3
    6. Vapor Pressure: 0.00146mmHg at 25°C
    7. Refractive Index: 1.586
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,3-DIHYDRO-1-BENZOFURAN-5-CARBONYL CHLORIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,3-DIHYDRO-1-BENZOFURAN-5-CARBONYL CHLORIDE(55745-71-6)
    12. EPA Substance Registry System: 2,3-DIHYDRO-1-BENZOFURAN-5-CARBONYL CHLORIDE(55745-71-6)

  • Safety Data

    1. Hazard Codes: C,Xn
    2. Statements: 34-51-22
    3. Safety Statements: 26-36/37/39-45
    4. RIDADR: 3261
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 55745-71-6(Hazardous Substances Data)

55745-71-6 Usage

Chemical Properties

white to light yellow crystal powde

Check Digit Verification of cas no

The CAS Registry Mumber 55745-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,4 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55745-71:
(7*5)+(6*5)+(5*7)+(4*4)+(3*5)+(2*7)+(1*1)=146
146 % 10 = 6
So 55745-71-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H7ClO2/c10-9(11)7-1-2-8-6(5-7)3-4-12-8/h1-2,5H,3-4H2

55745-71-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-DIHYDRO-1-BENZOFURAN-5-CARBONYL CHLORIDE

1.2 Other means of identification

Product number -
Other names ZLD0311

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:55745-71-6 SDS

55745-71-6Relevant articles and documents

Ruthenium-Catalyzed Difluoroalkylation of 8-Aminoquinoline Amides at the C5-Position

Chen, Changpeng,Zeng, Runsheng,Zhang, Jingyu,Zhao, Yingsheng

supporting information, p. 6947 - 6950 (2017/12/26)

A ruthenium-catalyzed highly selective difluoromethylation of 8-aminoquinoline amides at the C5 position has been developed. It tolerates a broad range of functional groups, providing the corresponding difluoromethylated products in moderate to good yields. Preliminary experimental results indicate that the tricoordinate ruthenium intermediate is the key factor in achieving the C5-position selectivity.

Heterocyclic N-acetonylbenzamides and their use as fungicides

-

Page 18, (2010/01/31)

Certain N-acetonylbenzamides and their use as fungicides are disclosed. The N-acetonylbenzamides disclosed contain a heterocyclic ring fused to an aromatic ring. These compounds are particularly effective against phytopathogenic fungi of the class Oomycetes. Also disclosed is a method for controlling phytopathogenic fungi by applying one or more of the heterocyclic N-acetonylbenzamides of the present invention, optionally with one or more additional fungicidal compounds.

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