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2689-65-8

5-Iodo-2-furancarboxaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 2689-65-8 Structure

  • Basic information

    1. Product Name: 5-Iodo-2-furancarboxaldehyde
    2. Synonyms: 5-Iodo-2-furaldehyde95%;OTAVA-BB BB7110951013;5-iodo-2-furaldehdye;5-IODO-2-FURALDEHYDE;5-IODO-2-FURANCARBOXALDEHYDE;5-IODOFURANCARBOXALDEHYDE;5-IODO-FURAN-2-CARBALDEHYDE;5-IODOFURAN-2-CARBOXALDEHYDE
    3. CAS NO:2689-65-8
    4. Molecular Formula: C5H3IO2
    5. Molecular Weight: 221.98
    6. EINECS: -0
    7. Product Categories: Miscellaneous;Building Blocks;Furans;FuransHeterocyclic Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks
    8. Mol File: 2689-65-8.mol

  • Chemical Properties

    1. Melting Point: 125-128 °C(lit.)
    2. Boiling Point: 274.5 °C at 760 mmHg
    3. Flash Point: 119.8 °C
    4. Appearance: light-yellow to orange crystalline powder
    5. Density: 2.094 g/cm3
    6. Vapor Pressure: 0.0054mmHg at 25°C
    7. Refractive Index: 1.64
    8. Storage Temp.: Refrigerator (+4°C)
    9. Solubility: soluble in Methanol
    10. Sensitive: Air & Light Sensitive
    11. BRN: 108406
    12. CAS DataBase Reference: 5-Iodo-2-furancarboxaldehyde(CAS DataBase Reference)
    13. NIST Chemistry Reference: 5-Iodo-2-furancarboxaldehyde(2689-65-8)
    14. EPA Substance Registry System: 5-Iodo-2-furancarboxaldehyde(2689-65-8)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37-37/39-36
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2689-65-8(Hazardous Substances Data)

2689-65-8 Usage

Chemical Properties

light-yellow to orange crystalline powder or

Check Digit Verification of cas no

The CAS Registry Mumber 2689-65-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,8 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2689-65:
(6*2)+(5*6)+(4*8)+(3*9)+(2*6)+(1*5)=118
118 % 10 = 8
So 2689-65-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H3IO2/c6-5-2-1-4(3-7)8-5/h1-3H

2689-65-8 Well-known Company Product Price

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  • Alfa Aesar

  • (L19670)  5-Iodo-2-furaldehyde, 97%   

  • 2689-65-8

  • 1g

  • 361.0CNY

  • Detail

  • Alfa Aesar

  • (L19670)  5-Iodo-2-furaldehyde, 97%   

  • 2689-65-8

  • 5g

  • 1605.0CNY

  • Detail

  • Aldrich

  • (579289)  5-Iodo-2-furaldehyde  97%

  • 2689-65-8

  • 579289-1G

  • 414.18CNY

  • Detail

2689-65-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-iodofuran-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-Iodofuran-2-carbaldehyde

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:2689-65-8 SDS

2689-65-8Relevant articles and documents

Reevaluation of benzyltrimethylammonium dichloroiodide, previously reported to be a selective iodinating agent

D'Auria,Mauriello

, p. 248 - 250 (2007/10/02)

Benzyltrimethylammonium dichloroiodate, previously reported as an iodinating agent of thiophenes, appears to be a selective chlorinating agent of both thienyl and furyl derivatives containing a carbonyl group.

Mechanism of the Reaction of Aldehydes of the Furan Series with Secondary Amines in Methanol

Novikov, V. N.,Borodaev, S. V.,Babeshkina, L. D.

, p. 448 - 454 (2007/10/02)

The reaction of 5-halofurfurals with piperidine and morpholine in methanol under various reaction conditions was investigated by means of spectrophotometry.The kinetics of the stepwise addition of the amine to the aldehyde function of the halofurfural were studied in the case of a dilute solution, while the conversion of the aldehyde to a 5-N,N-dialkylaminofurfurylidene-N,N-dialkylimmonium salt, for which two autocatalysis mechanisms were observed, was investigated in the case of a concentrated solution.Reaction intermediates, viz., 5-halofurfurylidene-N,N-bis(dialkylamines), were isolated preparatively and investigated.

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