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CAS

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10445-02-0

5-(3-(trifluoromethyl)phenyl)-1,3,4-thiadiazol-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10445-02-0 Structure

  • Basic information

    1. Product Name: 5-(3-(trifluoromethyl)phenyl)-1,3,4-thiadiazol-2-amine
    2. Synonyms: 5-(3-(trifluoromethyl)phenyl)-1,3,4-thiadiazol-2-amine
    3. CAS NO:10445-02-0
    4. Molecular Formula:
    5. Molecular Weight: 245.228
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10445-02-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-(3-(trifluoromethyl)phenyl)-1,3,4-thiadiazol-2-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(3-(trifluoromethyl)phenyl)-1,3,4-thiadiazol-2-amine(10445-02-0)
    11. EPA Substance Registry System: 5-(3-(trifluoromethyl)phenyl)-1,3,4-thiadiazol-2-amine(10445-02-0)

  • 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: 10445-02-0(Hazardous Substances Data)

10445-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10445-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,4 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10445-02:
(7*1)+(6*0)+(5*4)+(4*4)+(3*5)+(2*0)+(1*2)=60
60 % 10 = 0
So 10445-02-0 is a valid CAS Registry Number.

10445-02-0Relevant articles and documents

Synthesis of 2-amino-1,3,4-oxadiazoles and 2-Amino-1,3,4-thiadiazoles via sequential condensation and I2-mediated oxidative C-O/C-S bond formation

Niu, Pengfei,Kang, Jinfeng,Tian, Xianhai,Song, Lina,Liu, Hongxu,Wu, Jie,Yu, Wenquan,Chang, Junbiao

, p. 1018 - 1024 (2015)

2-Amino-substituted 1,3,4-oxadiazoles and 1,3,4-thiadiazoles were synthesized via condensation of semicarbazide/thiosemicarbazide and the corresponding aldehydes followed by I2-mediated oxidative C-O/C-S bond formation. This transition-metal-free sequential synthesis process is compatible with aromatic, aliphatic, and cinnamic aldehydes, providing facile access to a variety of diazole derivatives bearing a 2-amino substituent in an efficient and scalable fashion.

Antihypertensive Thiadiazoles. 1. Synthesis of Some 2-Aryl-5-hydrazino-1,3,4-thiadiazoles with Vasodilator Activity

Turner, Stephen,Myers, Malcolm,Gadie, Brian,Nelson, Anthony J.,Pape, Robin,et al.

, p. 902 - 906 (2007/10/02)

Some 2-Aryl-5-hydrazino-1,3,4-thiadiazoles have been synthesized and screened for antihypertensive activity.In general, compounds with a 2-substituted phenyl ring had higher activity than their 3- or 4-substituted counterparts or those containing heteroar

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