Welcome to LookChem.com Sign In|Join Free

CAS

  • or
3-Bromo-5-methylbenzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

188813-04-9 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 188813-04-9 Structure
  • Basic information

    1. Product Name: 3-Bromo-5-methylbenzaldehyde
    2. Synonyms: 3-Bromo-5-methylbenzaldehyde
    3. CAS NO:188813-04-9
    4. Molecular Formula: C8H7BrO
    5. Molecular Weight: 199.04458
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 188813-04-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 255.59 °C at 760 mmHg
    3. Flash Point: 91.22 °C
    4. Appearance: /
    5. Density: 1.49 g/cm3
    6. Vapor Pressure: 0.016mmHg at 25°C
    7. Refractive Index: 1.597
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-Bromo-5-methylbenzaldehyde(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-Bromo-5-methylbenzaldehyde(188813-04-9)
    12. EPA Substance Registry System: 3-Bromo-5-methylbenzaldehyde(188813-04-9)
  • 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: 188813-04-9(Hazardous Substances Data)

188813-04-9 Usage

Chemical Properties

Pale yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 188813-04-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,8,1 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 188813-04:
(8*1)+(7*8)+(6*8)+(5*8)+(4*1)+(3*3)+(2*0)+(1*4)=169
169 % 10 = 9
So 188813-04-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H7BrO/c1-6-2-7(5-10)4-8(9)3-6/h2-5H,1H3

188813-04-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromo-5-methylbenzaldehyde

1.2 Other means of identification

Product number -
Other names Benzaldehyde,3-bromo-5-methyl

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:188813-04-9 SDS

188813-04-9Relevant articles and documents

LIGHT INDUCED CATALYTIC C-H OXYGENATION OF ALKANES

-

Paragraph 00219, (2021/04/02)

A method of oxygenating a benzylic C-H bond is provided. The method comprises light induced activation of an initiator and subsequent reaction with oxygen, resulting in the formation of free radicals. Subsequently, free radicals catalyze the reaction of the benzylic C-H bond with oxygen, thereby forming an oxygenated compound.

Visible-Spectrum Solar-Light-Mediated Benzylic C-H Oxygenation Using 9,10-Dibromoanthracene As an Initiator

Santra, Sourav K.,Szpilman, Alex M.

, p. 1164 - 1171 (2020/12/23)

We report a visible-light-mediated benzylic C-H oxygenation reaction. The reaction is initiated by solar light or the blue LED activation of 9,10-dibromoanthracene in a reaction with oxygen and takes place at ambient temperature and air pressure. Secondary benzylic positions are oxygenated to ketones, while tertiary benzylic carbons are oxygenated to give hydroperoxides. Notably, cumene hydroperoxide is produced in a higher yield and at milder conditions than the currently employed industrial conditions.

Method for synthesizing aromatic aldehyde, aromatic ketone and aromatic ester through catalytically oxidizing alkyl aromatic compound by iron

-

Paragraph 0054; 0055, (2017/10/13)

The invention discloses a method for synthesizing aromatic aldehyde, aromatic ketone and aromatic ester through catalytically oxidizing an alkyl aromatic compound by iron, and belongs to the technical field of catalytic synthesis. According to the method, a low-cost and environment-friendly iron catalyst is used under a normal pressure; under the action of hydrogen and silicon reagents serving as an accelerant and an oxidant, a side chain of an aromatic hydrocarbon is oxidized into a carbonyl group for generating the corresponding aromatic aldehyde, aromatic ketone and aromatic ester. The method for preparing the aromatic aldehyde, the aromatic ketone and the aromatic ester through a catalytic oxidation reaction, which is provided by the invention, has numerous advantages that a catalyst, reaction raw materials, the oxidant and a silicon reagent are wide in sources and good in stability and is low-cost and environment-friendly; the alkyl aromatic compound is metered to participate in a reaction; the reaction condition is mild; the compatibility of functional groups is good; the scope of application is wide; the reaction selectivity is good; in an optimized reaction condition, the separation yield of a target product can be up to approximately 95 percent.

PYRIDONE DERIVATIVES AS NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS

-

Page/Page column 80, (2010/04/03)

The present invention relates to 2-pyridone derivatives of Formula (I) or (IV) as herein described, compositions containing such compounds, synthetic processes for making such compounds, and therapeutic methods that include the administration of such comp

Synthesis and structure-activity relationships of new disubstituted phenyl-containing 3,4-diamino-3-cyclobutene-1,2-diones as CXCR2 receptor antagonists

Lai, Gaifa,Merritt, J. Robert,He, Zhenmin,Feng, Daming,Chao, Jianhua,Czarniecki, Michael F.,Rokosz, Laura L.,Stauffer, Tara M.,Rindgen, Diane,Taveras, Arthur G.

, p. 1864 - 1868 (2008/12/21)

A series of 3,4- and 3,5-disubstituted phenyl-containing cyclobutenedione analogues were synthesized and evaluated as CXCR2 receptor antagonists. Variations in the disubstitution pattern of the phenyl ring afforded new compounds with potent CXCR2 binding

ENANTIOMERICALLY PURE PHOSPHOINDOLES AS HIV INHIBITORS

-

Page/Page column 133 - 134, (2008/06/13)

3-phosphoindole compounds substantially in the form of a single enantiomer useful for the treatment of Flaviviridae virus infections, and particularly for HIV infections are provided. Also provided are pharmaceutical compositions comprising the 3-phosphoi

Synthesis and characterization of aryl thioacetyl styrene monomers: towards a new generation of SERS-active polymers

Al-Hourani, Baker Jawabrah,Bravo-Vasquez, Juan P.,Hermann High,Fenniri, Hicham

, p. 9144 - 9147 (2008/09/17)

A new family of thioacetyl styrene derivatives was synthesized in good isolated yields for the preparation of spectroscopically-encoded SERS-active polymers.

META-GUANIDINE, UREA, THIOUREA OR AZACYCLIC AMINO BENZOIC ACID DERIVATIVES AS INTEGRIN ANTAGONISTS

-

, (2008/06/13)

The present invention relates to a class of compounds represented by the Formula Ior a pharmaceutically acceptable salt thereof, whereinA ispharmaceutical compositions thereof and methods of using such compounds and compositions as alphavbeta3 antagonists.

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 188813-04-9