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N-(6-amino-1,3-benzothiazol-2-yl)cyclohexanecarboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 313504-94-8 Structure
  • Basic information

    1. Product Name: N-(6-amino-1,3-benzothiazol-2-yl)cyclohexanecarboxamide
    2. Synonyms: N-(6-amino-1,3-benzothiazol-2-yl)cyclohexanecarboxamide
    3. CAS NO:313504-94-8
    4. Molecular Formula: C14H17N3OS
    5. Molecular Weight: 275.36928
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 313504-94-8.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: N-(6-amino-1,3-benzothiazol-2-yl)cyclohexanecarboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(6-amino-1,3-benzothiazol-2-yl)cyclohexanecarboxamide(313504-94-8)
    11. EPA Substance Registry System: N-(6-amino-1,3-benzothiazol-2-yl)cyclohexanecarboxamide(313504-94-8)
  • 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: 313504-94-8(Hazardous Substances Data)

313504-94-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 313504-94-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,5,0 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 313504-94:
(8*3)+(7*1)+(6*3)+(5*5)+(4*0)+(3*4)+(2*9)+(1*4)=108
108 % 10 = 8
So 313504-94-8 is a valid CAS Registry Number.

313504-94-8Relevant articles and documents

Synthesis and biological evaluation of a series of (Benzo[d]thiazol-2-yl) cyclohexanecarboxamides and (Benzo[d]thiazol-2-yl)cyclohexanecarbothioamides

Nam, Nguyen Hai,Dung, Phan Thi Phuong,Thuong, Phuong Thien,Hien, Tran Thi

experimental part, p. 159 - 164 (2011/08/10)

A series of benzothiazole derivatives including N-(benzo[d]thiazol-2-yl) cyclohexanecarboxamides (2a-g) and N-(benzo[d]thiazol-2-yl) cyclohexancarbothioamides (3b-d) have been synthesized and evaluated for cytotoxic and antimicrobial activities. Two compo

Synthesis and biological evaluation of benzothiazole derivatives as potent antitumor agents

Yoshida, Masao,Hayakawa, Ichiro,Hayashi, Noriyuki,Agatsuma, Toshinori,Oda, Youko,Tanzawa, Fumie,Iwasaki, Shiho,Koyama, Kumiko,Furukawa, Hidehiko,Kurakata, Shinichi,Sugano, Yuichi

, p. 3328 - 3332 (2007/10/03)

Based on 2-methyl-4-nitro-2H-pyrazole-3-carboxylic acid[2- (cyclohexanecarbonylamino)benzothiazol-6-yl]amide (1), which shows selective cytotoxicity against tumorigenic cell lines, 2,6-dichloro-N-[2- (cyclopropanecarbonylamino)benzothiazol-6-yl]benzamide (13b) was designed and synthesized as a biologically stable derivative containing no nitro group. The highly potent derivative 13b exhibited excellent in vivo inhibitory effect on tumor growth.

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