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6-Bromo-2-(4-chlorophenyl)-3-nitro-2H-1-benzopyran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 57544-18-0 Structure
  • Basic information

    1. Product Name: 6-Bromo-2-(4-chlorophenyl)-3-nitro-2H-1-benzopyran
    2. Synonyms: 6-Bromo-2-(4-chlorophenyl)-3-nitro-2H-1-benzopyran
    3. CAS NO:57544-18-0
    4. Molecular Formula: C15H9BrClNO3
    5. Molecular Weight: 366.59
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 57544-18-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 484.7°C at 760 mmHg
    3. Flash Point: 246.9°C
    4. Appearance: /
    5. Density: 1.69g/cm3
    6. Vapor Pressure: 4.46E-09mmHg at 25°C
    7. Refractive Index: 1.696
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 6-Bromo-2-(4-chlorophenyl)-3-nitro-2H-1-benzopyran(CAS DataBase Reference)
    11. NIST Chemistry Reference: 6-Bromo-2-(4-chlorophenyl)-3-nitro-2H-1-benzopyran(57544-18-0)
    12. EPA Substance Registry System: 6-Bromo-2-(4-chlorophenyl)-3-nitro-2H-1-benzopyran(57544-18-0)
  • 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: 57544-18-0(Hazardous Substances Data)

57544-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57544-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,4 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57544-18:
(7*5)+(6*7)+(5*5)+(4*4)+(3*4)+(2*1)+(1*8)=140
140 % 10 = 0
So 57544-18-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H9BrClNO3/c16-11-3-6-14-10(7-11)8-13(18(19)20)15(21-14)9-1-4-12(17)5-2-9/h1-8,15H

57544-18-0SDS

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-Bromo-2-(4-chlorophenyl)-3-nitro-2H-chromene

1.2 Other means of identification

Product number -
Other names 2H-1-BENZOPYRAN,6-BROMO-2-(4-CHLOROPHENYL)-3-NITRO

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:57544-18-0 SDS

57544-18-0Downstream Products

57544-18-0Relevant articles and documents

Molecular diversity of the domino annulation reaction of 2-aryl-3-nitrochromenes with pivaloylacetonitriles

Jiang, Wang,Sun, Jing,Liu, Ru-Zhang,Yan, Chao-Guo

supporting information, p. 5816 - 5822 (2018/08/21)

In the presence of triethylamine, the domino annulation reaction of two molecules of pivaloylacetonitrile with one molecule of 2-aryl-3-nitrochromene in tetrahydrofuran resulted in the unprecedented imino-substituted dihydrofuro[2,3-c]chromene derivatives in high yields. More importantly, the above domino reaction in refluxing methanol or ethanol afforded alkoxy-substituted chromeno[3,4-b]pyridines in satisfactory yields. However, a similar reaction of benzoylacetonitrile with 2-aryl-3-nitrochromenes in basic medium gave the expected furo[2,3-c]chromene derivatives in moderate yields.

NEW PI3K/AKT/MTOR INHIBITORS AND PHARMACEUTICAL USES THEREOF

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Page/Page column 28; 35; 36, (2015/04/15)

The invention relates to new PI3K/AKT/m TOR inhibitors and their use for the prevention and/or the treatment of a disease selected from the group consisting of: inflammatory diseases, autoimmune diseases, neurodegenerative diseases, cancers, transplant re

New PI3K/AKT/mTOR inhibitors and pharmaceutical uses thereof

-

Paragraph 0096; 0099, (2015/04/15)

The invention relates to new PI3K/AKT/mTOR inhibitors of formula (I) and their use for the prevention and/or the treatment of a disease selected from the group consisting of: inflammatory diseases, autoimmune diseases, neurodegenerative diseases, cancers, transplant rejection, diseases characterized by a premature aging and tuberous sclerosis.

A Novel Covalent mTOR Inhibitor, DHM25, Shows in Vivo Antitumor Activity against Triple-Negative Breast Cancer Cells

Fouqué, Amélie,Delalande, Olivier,Jean, Mickael,Castellano, Rémy,Josselin, Emmanuelle,Malleter, Marine,Shoji, Kenji F.,Hung, Mac Dinh,Rampanarivo, Hariniaina,Collette, Yves,Van De Weghe, Pierre,Legembre, Patrick

supporting information, p. 6559 - 6573 (2015/09/07)

Constitutive activation of the PI3K/mTOR signaling pathway contributes to carcinogenesis and metastasis in most, if not all, breast cancers. From a chromene backbone reported to inhibit class I PI3K catalytic subunits, several rounds of chemical syntheses led to the generation of a new collection of chromologues that showed enhanced ability to kill PI3K-addicted cancer cells and to inhibit Akt phosphorylation at serine 473, a hallmark of PI3K/mTOR activation. This initial screen uncovered a chromene designated DHM25 that exerted potent antitumor activity against breast tumor cell lines. Strikingly, DHM25 was shown to be a selective and covalent inhibitor of mTOR using biochemical and cellular analyses, modeling, and a large panel of kinase activity assays spanning the human kinome (243 kinases). Finally, in vivo, this novel drug was an efficient inhibitor of growth and metastasis of triple-negative breast cancer cells, paving the way for its clinical application in oncology. (Figure Presented).

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