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2-Benzothiazolecarbonitrile,6-fluoro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 169776-04-9 Structure
  • Basic information

    1. Product Name: 2-Benzothiazolecarbonitrile,6-fluoro-(9CI)
    2. Synonyms: 2-Benzothiazolecarbonitrile,6-fluoro-(9CI);2-Benzothiazolecarbonitrile,6-fluoro-
    3. CAS NO:169776-04-9
    4. Molecular Formula: C8H3FN2S
    5. Molecular Weight: 178.19
    6. EINECS: N/A
    7. Product Categories: BENZOTHIAZOLE
    8. Mol File: 169776-04-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Benzothiazolecarbonitrile,6-fluoro-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Benzothiazolecarbonitrile,6-fluoro-(9CI)(169776-04-9)
    11. EPA Substance Registry System: 2-Benzothiazolecarbonitrile,6-fluoro-(9CI)(169776-04-9)
  • 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: 169776-04-9(Hazardous Substances Data)

169776-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169776-04-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,7,7 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 169776-04:
(8*1)+(7*6)+(6*9)+(5*7)+(4*7)+(3*6)+(2*0)+(1*4)=189
189 % 10 = 9
So 169776-04-9 is a valid CAS Registry Number.

169776-04-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-fluorobenzothiazole-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 6-Fluoro-benzothiazole-2-carbonitrile

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:169776-04-9 SDS

169776-04-9Downstream Products

169776-04-9Relevant articles and documents

Rapid Access to a Broad Range of 6′-Substituted Firefly Luciferin Analogues Reveals Surprising Emitters and Inhibitors

Sharma, Deepak K.,Adams, Spencer T.,Liebmann, Kate L.,Miller, Stephen C.

, p. 5836 - 5839 (2017/11/10)

Light-emitting firefly luciferin analogues contain electron-donating groups in the 6′-position, but the scope of known 6′-substitution remains narrow. A two-step route to a broad range of 6′-substituted luciferin analogues was developed to fill this void and enable more extensive study of the 6′-functionality. This chemistry allowed direct access to "caged" amide and bright azetidine analogues, but also revealed thioether inhibitors and unexpectedly luminogenic aryl amine derivatives.

Some chemistry of 4,5-dichloro-1,2,3-dithiazolium chloride and its derivatives

Besson, Thierry,Rees, Charles W.

, p. 1659 - 1662 (2007/10/02)

4,5-Dichloro-1,2,3-dithiazolium chloride 1 reacts with fluoroanilines (see Table 1) to give the iminodithiazoles 5 in very high yield.Thermolysis of the latter gave the corresponding 2-cyanobenzothiazoles 6 together, in some cases, with the cyanoimidoyl chlorides 7.This reaction sequence provides modest yields of 2-cyanobenzothiazoles from the corresponding aniline, in two steps.Treatment of the iminodithiazoles with m-chloroperbenzoic acid in dichloromethane at or below room temperature opened the heterocyclic ring to give the N-arylcyanothioformamides (e.g. 8 --> 10), except for the p-nitrophenyl compound which gave p-nitrophenyl isothiocyanate 14 in high yield.

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