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690634-08-3

N-(FURAN-2-YLMETHYL)-1H-BENZOTRIAZOLE-1& is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 690634-08-3 Structure

  • Basic information

    1. Product Name: N-(FURAN-2-YLMETHYL)-1H-BENZOTRIAZOLE-1&
    2. Synonyms: N-(FURAN-2-YLMETHYL)-1H-BENZOTRIAZOLE-1&
    3. CAS NO:690634-08-3
    4. Molecular Formula: C12H10N4OS
    5. Molecular Weight: 258.304
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 690634-08-3.mol

  • Chemical Properties

    1. Melting Point: 119-127 °C
    2. Boiling Point: 434.3±47.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.43±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 9.47±0.70(Predicted)
    10. CAS DataBase Reference: N-(FURAN-2-YLMETHYL)-1H-BENZOTRIAZOLE-1&(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-(FURAN-2-YLMETHYL)-1H-BENZOTRIAZOLE-1&(690634-08-3)
    12. EPA Substance Registry System: N-(FURAN-2-YLMETHYL)-1H-BENZOTRIAZOLE-1&(690634-08-3)

  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22-37/38-41
    3. Safety Statements: 26-36/37/39
    4. WGK Germany: -
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 690634-08-3(Hazardous Substances Data)

690634-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 690634-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,0,6,3 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 690634-08:
(8*6)+(7*9)+(6*0)+(5*6)+(4*3)+(3*4)+(2*0)+(1*8)=173
173 % 10 = 3
So 690634-08-3 is a valid CAS Registry Number.

690634-08-3SDS

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 N-(furan-2-ylmethyl)benzotriazole-1-carbothioamide

1.2 Other means of identification

Product number -
Other names 1H-BENZOTRIAZOLE-1-CARBOTHIOAMIDE,N-(2-FURANYLMETHYL)

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:690634-08-3 SDS

690634-08-3Downstream Products

690634-08-3Relevant articles and documents

Convenient one-pot synthesis of 5-(Substituted amino)-1,2,3,4-thiatriazoles

Katritzky, Alan R.,Meher, Geeta,Narindoshvili, Tamari

experimental part, p. 1061 - 1068 (2010/04/26)

5-(Substituted amino)-1,2,3,4-thiatriazoles 15a-15i were conveniently synthesized in 73-97% yields in a one-pot procedure from bis(1H-benzotriazol-1- yl)methanethione and amines.

Benzotriazole-assisted thioacylation

Katritzky, Alan R.,Witek, Rachel M.,Rodriguez-Garcia, Valerie,Mohapatra, Prabhu P.,Rogers, James W.,Cusido, Janet,Abdel-Fattah, Ashraf A. A.,Steel, Peter J.

, p. 7866 - 7881 (2007/10/03)

Benzotriazole reagents for thioacylation (RCSBt), thiocarbamoylation (RR'NCSBt), aryl/alkoxy-thioacylation (ROCSBt), and aryl/alkylthiothioacylation (RSCSBt) are synthesized, and their utility is assessed by syntheses of representative heteroaryl thioureas 3a-g, thioamides 15a-s, thionoesters 16a-h, thiocarbamates 17a-e, dithiocarbamates 18a-d, thiocarbonates 19a-c, and dithiocarbonates 20a-c.

1-(Alkyl/Arylthiocarbamoyl)benzotriazoles as Stable Isothiocyanate Equivalents: Synthesis of Di- and Trisubstituted Thioureas

Katritzky, Alan R.,Ledoux, Stephane,Witek, Rachel M.,Nair, Satheesh K.

, p. 2976 - 2982 (2007/10/03)

1-(Alkyl/arylthiocarbamoyl)benzotriazoles 4a-i were synthesized in yields of 91-99% from bis(benzotriazolyl)methanethione (3). Reagents 4a-g were then used as isothiocyanate equivalents for the efficient synthesis of 10 secondary and 14 tertiary thioureas

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