Welcome to LookChem.com Sign In|Join Free

CAS

  • or
4-Bromo-2-(bromomethyl)-1-methoxybenzene, with the molecular formula C8H8Br2O, is an aromatic organic compound that falls under the category of benzene and its substituted derivatives. 4-BROMO-2-(BROMOMETHYL)-1-METHOXYBENZENE is characterized by the presence of two bromine atoms, one at the fourth carbon and the other on the methylene carbon, along with a methoxy group attached to the first carbon of the benzene ring. Due to the scarcity of data on its properties such as melting point, boiling point, density, or toxicity, it appears that this compound is not widely used or has been the subject of limited research. Further investigation may be necessary to gain a comprehensive understanding of its potential applications and characteristics.

184970-28-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 184970-28-3 Structure
  • Basic information

    1. Product Name: 4-BROMO-2-(BROMOMETHYL)-1-METHOXYBENZENE
    2. Synonyms: 4-BROMO-2-(BROMOMETHYL)-1-METHOXYBENZENE;4-Bromo-2-bromomethylanisole
    3. CAS NO:184970-28-3
    4. Molecular Formula: C8H8Br2O
    5. Molecular Weight: 279.96
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 184970-28-3.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.: Inert atmosphere,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-BROMO-2-(BROMOMETHYL)-1-METHOXYBENZENE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-BROMO-2-(BROMOMETHYL)-1-METHOXYBENZENE(184970-28-3)
    11. EPA Substance Registry System: 4-BROMO-2-(BROMOMETHYL)-1-METHOXYBENZENE(184970-28-3)
  • 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: 184970-28-3(Hazardous Substances Data)

184970-28-3 Usage

Uses

Due to the limited available data on 4-BROMO-2-(BROMOMETHYL)-1-METHOXYBENZENE, its specific applications are not clearly outlined in the provided materials. However, given its chemical structure and the presence of bromine and methoxy groups, it can be inferred that this compound may have potential uses in various industries, such as:
Used in Chemical Synthesis Industry:
4-BROMO-2-(BROMOMETHYL)-1-METHOXYBENZENE could be used as an intermediate or a building block in the synthesis of more complex organic compounds, particularly those requiring bromine and methoxy functionalities.
Used in Pharmaceutical Industry:
Given the presence of bromine and methoxy groups, 4-BROMO-2-(BROMOMETHYL)-1-METHOXYBENZENE might be utilized in the development of new pharmaceutical compounds, where these functional groups could contribute to the desired biological activity or improve the drug's pharmacokinetic properties.
Used in Material Science:
4-BROMO-2-(BROMOMETHYL)-1-METHOXYBENZENE's aromatic structure and bromine content could make it a candidate for the development of new materials with specific properties, such as flame retardancy or enhanced thermal stability.

Check Digit Verification of cas no

The CAS Registry Mumber 184970-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,9,7 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 184970-28:
(8*1)+(7*8)+(6*4)+(5*9)+(4*7)+(3*0)+(2*2)+(1*8)=173
173 % 10 = 3
So 184970-28-3 is a valid CAS Registry Number.

184970-28-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-BROMO-2-(BROMOMETHYL)-1-METHOXYBENZENE

1.2 Other means of identification

Product number -
Other names 4-Bromo-2-bromomethyl-1-methoxy-benzene

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:184970-28-3 SDS

184970-28-3Relevant articles and documents

Synthesis and Evaluation of Europium Complexes that Switch on Luminescence in Lysosomes of Living Cells

Starck, Matthieu,Fradgley, Jack D.,Pal, Robert,Zwier, Jurriaan M.,Lamarque, Laurent,Parker, David

, p. 766 - 777 (2021)

A set of four luminescent EuIII complexes bearing an extended aryl-alkynylpyridine chromophore has been studied, showing very different pH-dependent behaviour in their absorption and emission spectral response. For two complexes with pKa/

PYRIMIDINE COMPOUNDS CONTAINING ACIDIC GROUPS

-

Paragraph 1052; 1053, (2018/06/15)

The present disclosure relates to a class of pyrimidine derivatives having immunomodulating properties that act via TLR7 which are useful in the treatment of viral infections and cancers.

One-pot transformation of methylarenes into aromatic aldehydes under metal-free conditions

Tabata, Masayuki,Moriyama, Katsuhiko,Togo, Hideo

, p. 3402 - 3410 (2014/06/09)

On the basis of studies of the transformation of benzylic bromides into the corresponding aromatic aldehydes by treatment with N-methylmorpholine N-oxide, various methylarenes were treated either with DBDMH in the presence of AIBN in acetonitrile at reflux (Method A) or with NBS in CCl4 under irradiation with a tungsten lamp at 30 °C (Method B), followed by treatment with N-methylmorpholine N-oxide to provide aromatic aldehydes in good yields. These methods could be adopted in one-pot transformations of methylarenes into aromatic aldehydes under conditions free of less toxic reagents and transition metals. Copyright

TRIAZOLONE COMPOUNDS AND USES THEREOF

-

Paragraph 00123; 00126; 00127, (2013/09/26)

The invention disclosed herein is directed to compounds of Formula (I) and pharmaceutically acceptable salts thereof, which are useful in the treatment of prostate, breast, colon, pancreatic, human chronic lymphocytic leukemia, melanoma and other cancers. The invention also comprises pharmaceutical compositions comprising a therapeutically effective amount of compound of Formula (I), or a pharmaceutically acceptable salt thereof. The invention disclosed herein is also directed to methods of treating prostate, breast, ovarian, liver, kidney, colon, pancreatic, human chronic lymphocytic leukemia, melanoma and other cancers. The invention disclosed herein is further directed to methods of treating prostate, breast, colon, pancreatic, chronic lymphocytic leukemia, melanoma and other cancers comprising administration of a of a therapeutically effective amount of a selective PPARα antagonist. The compounds and pharmaceutical compositions of the invention are also useful in the treatment of viral infections, such as HCV infections and HIV infections. The invention disclosed herein is also directed to a methods of preventing the onset of and/or recurrence of acute and chronic myeloid leukemia, as well as other cancers, comprising administration of a of a therapeutically effective amount of a selective PPARα antagonist.

Direct oxidative conversion of methylarenes into aromatic nitriles

Tsuchiya, Daisuke,Kawagoe, Yuhsuke,Moriyama, Katsuhiko,Togo, Hideo

supporting information, p. 4194 - 4197 (2013/09/12)

A variety of methylarenes were successfully converted into the corresponding aromatic nitriles in good to moderate yields by the treatment with NBS or DBDMH in the presence of a catalytic amount of AIBN or BPO, followed by the reaction with molecular iodine in aq NH3 in a one-pot procedure. The present reaction is a useful and practical transition-metal-free method for the preparation of aromatic nitriles from methylarenes.

A concise synthesis of 4′-O-methyl honokiol

Denton, Ross M.,Scragg, James T.,Saska, Jan

supporting information; experimental part, p. 2554 - 2556 (2011/06/21)

A concise and protecting group free synthesis of the naturally occurring neolignan 4′-O-methyl honokiol is developed. The key biaryl bond is constructed by 1,2-addition of an aryl Grignard reagent to a dienone followed by rearrangement.

NK-1 AND SEROTONIN TRANSPORTER INHIBITORS

-

Page/Page column 73, (2010/11/28)

The invention encompasses compounds of Formula I, including pharmaceutically acceptable salts, their pharmaceutical compositions, and their use in treating disorders associated with an excess or imbalance of tachykinins or serotonin or both.

1-BENZYLINDOLE-2-CARBOXAMIDE DERIVATIVES

-

Page/Page column 32, (2010/11/24)

The present invention relates to i-benzylindole-2-carboxamide derivatives of formula I, or a pharmaceutically acceptable salt or solvate thereof. The invention also relates to pharmaceutical compositions comprising said 1-benzylindole-2-carboxamide deriva

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 184970-28-3