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1-CARBAZOL-9-YL-3-METHYLAMINO-PROPAN-2-OL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 701226-41-7 Structure
  • Basic information

    1. Product Name: 1-CARBAZOL-9-YL-3-METHYLAMINO-PROPAN-2-OL
    2. Synonyms: 1-CARBAZOL-9-YL-3-METHYLAMINO-PROPAN-2-OL;TIMTEC-BB SBB011986
    3. CAS NO:701226-41-7
    4. Molecular Formula: C16H18N2O
    5. Molecular Weight: 254.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 701226-41-7.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: 1-CARBAZOL-9-YL-3-METHYLAMINO-PROPAN-2-OL(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-CARBAZOL-9-YL-3-METHYLAMINO-PROPAN-2-OL(701226-41-7)
    11. EPA Substance Registry System: 1-CARBAZOL-9-YL-3-METHYLAMINO-PROPAN-2-OL(701226-41-7)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 701226-41-7(Hazardous Substances Data)

701226-41-7 Usage

Chemical class

Carbazole derivatives

Structure

Carbazole ring with a 3-methylamino-propan-2-ol substituent

Potential applications

Pharmaceutical and organic synthesis

Research and development

Used in the development of novel compounds with therapeutic properties

Biological activity

May possess biological activity

Building block

Could be used as a building block for the synthesis of new compounds

Further investigation

Specific properties and uses need to be investigated
Please note that this list is based on the provided material and may not be exhaustive. Further research and investigation are required to fully understand the properties and potential applications of 1-CARBAZOL-9-YL-3-METHYLAMINO-PROPAN-2-OL.

Check Digit Verification of cas no

The CAS Registry Mumber 701226-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,1,2,2 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 701226-41:
(8*7)+(7*0)+(6*1)+(5*2)+(4*2)+(3*6)+(2*4)+(1*1)=107
107 % 10 = 7
So 701226-41-7 is a valid CAS Registry Number.

701226-41-7Downstream Products

701226-41-7Relevant articles and documents

Identification of racemic and chiral carbazole derivatives containing an isopropanolamine linker as prospective surrogates against plant pathogenic bacteria: In vitro and in vivo assays and quantitative proteomics

Zhao, Yong-Liang,Huang, Xing,Liu, Li-Wei,Wang, Pei-Yi,Long, Qing-Su,Tao, Qing-Qing,Li, Zhong,Yang, Song

, p. 7512 - 7525 (2019/08/21)

Recent observations on the emergence of drug-resistant plant pathogenic bacteria have highlighted and elicited an acute campaign to develop novel, highly efficient antibiotic surrogates for managing bacterial diseases in agriculture. Thus, a type of racemic and chiral carbazole derivative containing an isopropanolamine pattern was systematically synthesized to discover low-cost and efficient antibacterial candidates. Screening results showed that compounds 2f, 6c, and 2j could significantly suppress the growth of tested plant pathogens, namely Xanthomonas oryzae pv oryzae, X. axonopodis pv citri, and Pseudomonas syringae pv actinidiae, and provided the corresponding EC50 values of 1.27, 0.993, and 0.603 μg/mL, which were significantly better than those of existing commercial drugs. In vivo studies confirmed their prospective applications for controlling plant bacterial diseases. Label-free quantitative proteomics analysis indicated that compound 2f could dramatically induce the up- and down-regulation of a total of 247 differentially expressed proteins, which was further validated by the parallel reaction monitoring technique. Moreover, fluorescence spectra and SEM images were obtained to further explore the antibacterial mechanism.

With chiral center carbazolyl isopropanolamine derivatives of the preparation method and application of (by machine translation)

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Paragraph 0058; 0059; 0060; 0062; 0070, (2019/05/04)

The invention relates to a with chiral center carbazolyl isopropanolamine derivatives of the preparation method and application. This compound has the general formula (I) indicated by the structure: The compound such as [...] Phaeosphaeria, tobacco wilt b

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