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

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  • 1544-85-0 Structure
  • Basic information

    1. Product Name: 2,2-Difluoro-5-aminobenzodioxole
    2. Synonyms: IFLAB-BB F2108-0168;2,2-DIFLUORO-5-AMINOBENZODIOXOLE;2,2-DIFLUORO-5-AMINO-1,3-BENZODIOXOLE;2,2-DIFLUORO-BENZO[1,3]DIOXOL-5-YLAMINE;5-AMINO-2,2-DIFLUORO-1,3-BENZODIOXOLE;5-AMINO-2,2-DIFLUOROBENZODIOXOLE;3,4-[(Difluoromethylene)dioxy]aniline;5-Amino-2,2-difluoro-1,3-benzodioxole, 97+%
    3. CAS NO:1544-85-0
    4. Molecular Formula: C7H5F2NO2
    5. Molecular Weight: 173.12
    6. EINECS: -0
    7. Product Categories: Heterocycles series
    8. Mol File: 1544-85-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 95-97°C 12mm
    3. Flash Point: 95-97°C/12mm
    4. Appearance: /
    5. Density: 1.51 g/cm3
    6. Vapor Pressure: 0.0208mmHg at 25°C
    7. Refractive Index: 1.498
    8. Storage Temp.: Room temperature.
    9. Solubility: N/A
    10. PKA: 4.18±0.40(Predicted)
    11. Water Solubility: Not miscible or difficult to mix in water.
    12. Sensitive: Light Sensitive
    13. BRN: 1343593
    14. CAS DataBase Reference: 2,2-Difluoro-5-aminobenzodioxole(CAS DataBase Reference)
    15. NIST Chemistry Reference: 2,2-Difluoro-5-aminobenzodioxole(1544-85-0)
    16. EPA Substance Registry System: 2,2-Difluoro-5-aminobenzodioxole(1544-85-0)
  • Safety Data

    1. Hazard Codes: T,Xi
    2. Statements: 20/21/22-36/37/38-52-43-36
    3. Safety Statements: 26-36/37/39-36/37
    4. RIDADR: 2811
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: 6.1
    8. PackingGroup: III
    9. Hazardous Substances Data: 1544-85-0(Hazardous Substances Data)

1544-85-0 Usage

Uses

5-Amino-2,2-difluoro-1,3-benzodioxole is used as a pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 1544-85-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,4 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1544-85:
(6*1)+(5*5)+(4*4)+(3*4)+(2*8)+(1*5)=80
80 % 10 = 0
So 1544-85-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H5F2NO3/c8-7(9)13-6-3-1-5(2-4-6)10(11)12/h1-4,7H

1544-85-0 Well-known Company Product Price

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  • Alfa Aesar

  • (B24336)  5-Amino-2,2-difluoro-1,3-benzodioxole, 97+%   

  • 1544-85-0

  • 1g

  • 546.0CNY

  • Detail
  • Alfa Aesar

  • (B24336)  5-Amino-2,2-difluoro-1,3-benzodioxole, 97+%   

  • 1544-85-0

  • 5g

  • 1916.0CNY

  • Detail

1544-85-0SDS

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 2,2-Difluorobenzo[d][1,3]dioxol-5-amine

1.2 Other means of identification

Product number -
Other names 2,2-difluoro-1,3-benzodioxol-5-amine

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:1544-85-0 SDS

1544-85-0Relevant articles and documents

Bactericide and application thereof

-

Paragraph 0050; 0053; 0055, (2019/01/23)

The invention relates to the technical field of agriculture, in particular to a bactericide. The bactericide comprises a compound in a formula (A) as shown in the specification, wherein X1 and X2 areselected from fluorine and chlorine and can be identical or different, R1 and R2 are selected from aliphatic alkyls in carbon number of 1-20 and aryls formed by carbon and hydrogen and in carbon number of 6-20, and R is selected from aliphatic alkyls in carbon number of 1-20.

Bactericide and application thereof

-

Paragraph 0043; 0044; 0047-0050, (2019/02/03)

The invention relates to the technical field of agriculture, in particular to a bactericide. The bactericide comprises a compound show as the formula (A) (as described in the specification), wherein X1 and X2 are selected from fluorine and chlorine, and X1 and X2 can be same or different; and R1 and R2 are selected from aliphatic alkyl groups with 1 to 20 carbon atoms, and aryl groups (comprisingcarbon and hydrogen) with 6 to 20 carbon atoms.

Sterilizing agent and application thereof

-

Paragraph 0043-0044; 0047, (2019/01/13)

The invention relates to the technical field of agriculture, in particular to a sterilizing agent. The sterilizing agent comprises a compound as shown in formula (A): (shown in the description), wherein X1 and X2 are selected from fluorine; and R1 and R2 are selected from methyl, ethyl, propyl, butyl, amyl, hexyl and phenyl.

AMINATION AND HYDROXYLATION OF ARYLMETAL COMPOUNDS

-

Paragraph 0098; 0134; 0135; 0203, (2018/03/25)

In one aspect, the present disclosure provides methods of preparing a primary or secondary amine and hydroxylated aromatic compounds. In some embodiments, the aromatic compound may be unsubstituted, substituted, or contain one or more heteroatoms within the rings of the aromatic compound. The methods described herein may be carried out without the need for transition metal catalysts or harsh reaction conditions.

TYK2 INHIBITORS AND USES THEREOF

-

Paragraph 0895; 0896; 0897, (2016/09/26)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of TYK2, and the treatment of TYK2-mediated disorders.

Constructing the OCF2O moiety using BrF3

Hagooly, Youlia,Rozen, Shlomo

, p. 6780 - 6783 (2008/12/22)

(Chemical Equation Presented) A general preparation for aromatic and aliphatic, cyclic as well as linear, symmetric and asymmetric difluoromethylenedioxy derivatives is described. The alcohols were reacted with thiophosgene to give thiocarbonates, which in turn were reacted with BrF 3. The fluorination step is complete in seconds with moderate to high yields under mild conditions.

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