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29270-55-1

4-FLUORO-2,1,3-BENZOXADIAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 29270-55-1 Structure

  • Basic information

    1. Product Name: 4-FLUORO-2,1,3-BENZOXADIAZOLE
    2. Synonyms: 4-Fluoro-2,1,3-benzoxadiazole, HPLC 98%;4-fluorobenzo[c][1,2,5]oxadiazole;4-FLUORO-2,1,3-BENZOXADIAZOLE;4-Fluorobenzofurazan;4-fluoro-2,1,3-benzoxodiazole;4-Fluoro-2,1,3-benzoxadiazol
    3. CAS NO:29270-55-1
    4. Molecular Formula: C6H3FN2O
    5. Molecular Weight: 138.1
    6. EINECS: N/A
    7. Product Categories: Fluorescent Labels and Indicators;Fluorescent Labels & Indicators;MTS & Sulfhydryl Active Reagents;Aromatics;Heterocycles
    8. Mol File: 29270-55-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 83 °C / 12mmHg
    3. Flash Point: 69.8°C
    4. Appearance: /
    5. Density: 1.423g/cm3
    6. Vapor Pressure: 0.704mmHg at 25°C
    7. Refractive Index: 1.5250 to 1.5290
    8. Storage Temp.: Amber Vial, Refrigerator
    9. Solubility: Chloroform (Slightly), Dichloromethane (Slightly), Ethanol (Slightly), Ethyl Ace
    10. PKA: -1.81±0.45(Predicted)
    11. Stability: Light Sensitive
    12. CAS DataBase Reference: 4-FLUORO-2,1,3-BENZOXADIAZOLE(CAS DataBase Reference)
    13. NIST Chemistry Reference: 4-FLUORO-2,1,3-BENZOXADIAZOLE(29270-55-1)
    14. EPA Substance Registry System: 4-FLUORO-2,1,3-BENZOXADIAZOLE(29270-55-1)

  • 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: 29270-55-1(Hazardous Substances Data)

29270-55-1 Usage

Chemical Properties

Light Yellow Oil

Uses

A fluorescence benzofurazan derivative.

Check Digit Verification of cas no

The CAS Registry Mumber 29270-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,7 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29270-55:
(7*2)+(6*9)+(5*2)+(4*7)+(3*0)+(2*5)+(1*5)=121
121 % 10 = 1
So 29270-55-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H3FN2O/c7-4-2-1-3-5-6(4)9-10-8-5/h1-3H

29270-55-1 Well-known Company Product Price

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  • Detail

  • TCI America

  • (F0702)  4-Fluoro-2,1,3-benzoxadiazole  >98.0%(GC)

  • 29270-55-1

  • 1g

  • 990.00CNY

  • Detail

  • TCI America

  • (F0702)  4-Fluoro-2,1,3-benzoxadiazole  >98.0%(GC)

  • 29270-55-1

  • 5g

  • 3,380.00CNY

  • Detail

29270-55-1SDS

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 4-FLUORO-2,1,3-BENZOXADIAZOLE

1.2 Other means of identification

Product number -
Other names 4-Fluorobenzo[c][1,2,5]oxadiazole

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:29270-55-1 SDS

29270-55-1Relevant articles and documents

Revisiting the Synthesis of 4,6-Difluorobenzofuroxan: A Study of Its Reactivity and Access to Fluorinated Quinoxaline Oxides

Jovené, Cyril,Jacquet, Morgane,Marrot, Jérome,Bourdreux, Flavien,Kletsky, Mikhail E.,Burov, Oleg N.,Gon?alves, Anne-Marie,Goumont, Régis

, p. 6451 - 6466 (2016/02/18)

New quinoxaline 1,4-dioxide derivatives have been synthesized from novel fluorinated benzofuroxans such as 4-fluorobenzofuroxan, which is prepared for the first time. Furthermore, the preparation 4,6-difluorobenzofuroxan has been revisited because we were

Improved synthesis of 4-amino-7-nitrobenz-2,1,3-oxadiazoles using NBD fluoride (NBD-F)

Jung, Michael E.,Dong, Timothy A.,Cai, Xiaolu

supporting information; experimental part, p. 2533 - 2535 (2011/06/21)

The 7-nitrobenz-2,1,3-oxadiazole (NBD) unit is a highly useful fluorescent tag with wide application in biology. Installation of the NBD group typically proceeds via the SNAr reaction between an amine and an NBD halide. Herein, we demonstrate that NBD-F 1 results in significantly higher yields than NBD-Cl 2, and that triethylamine in dimethylformamide at 23 °C overnight is a broadly applicable set of conditions for this reaction. In particular, the highly useful fluorescent carbohydrate 2-NBD-glucosamine (2-NBDG, 3) can now be prepared in 75% yield with NBD-F as compared to 12% with NBD-Cl.

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