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4-BROMO-3-CHLOROBENZOIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 25118-59-6 Structure
  • Basic information

    1. Product Name: 4-BROMO-3-CHLOROBENZOIC ACID
    2. Synonyms: 3-chloro-4-Bromor-benzoic acid
    3. CAS NO:25118-59-6
    4. Molecular Formula: C7H4BrClO2
    5. Molecular Weight: 235.47
    6. EINECS: N/A
    7. Product Categories: C7;Carbonyl Compounds;Carboxylic Acids;intermediate
    8. Mol File: 25118-59-6.mol
  • Chemical Properties

    1. Melting Point: 220-224 °C
    2. Boiling Point: 333.686 °C at 760 mmHg
    3. Flash Point: 155.608 °C
    4. Appearance: /
    5. Density: 1.809±0.06 g/cm3 (20 ºC 760 Torr)
    6. Vapor Pressure: 5.32E-05mmHg at 25°C
    7. Refractive Index: 1.621
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: soluble in Methanol
    10. PKA: 3.60±0.10(Predicted)
    11. CAS DataBase Reference: 4-BROMO-3-CHLOROBENZOIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-BROMO-3-CHLOROBENZOIC ACID(25118-59-6)
    13. EPA Substance Registry System: 4-BROMO-3-CHLOROBENZOIC ACID(25118-59-6)
  • Safety Data

    1. Hazard Codes: Xn,N,Xi
    2. Statements: 22-50/53
    3. Safety Statements: 60-61
    4. RIDADR: UN 2811 6.1/PG 3
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: IRRITANT
    8. PackingGroup:
    9. Hazardous Substances Data: 25118-59-6(Hazardous Substances Data)

25118-59-6 Usage

Chemical Properties

White solid

Check Digit Verification of cas no

The CAS Registry Mumber 25118-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,1 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25118-59:
(7*2)+(6*5)+(5*1)+(4*1)+(3*8)+(2*5)+(1*9)=96
96 % 10 = 6
So 25118-59-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrClO2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3H,(H,10,11)

25118-59-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H27252)  4-Bromo-3-chlorobenzoic acid, 97%   

  • 25118-59-6

  • 5g

  • 778.0CNY

  • Detail
  • Alfa Aesar

  • (H27252)  4-Bromo-3-chlorobenzoic acid, 97%   

  • 25118-59-6

  • 25g

  • 2914.0CNY

  • Detail

25118-59-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-BROMO-3-CHLOROBENZOIC ACID

1.2 Other means of identification

Product number -
Other names Benzoic acid, 4-bromo-3-chloro-

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:25118-59-6 SDS

25118-59-6Relevant articles and documents

Method for preparing normal 2-docodone intermediate (I)-(C)-( -4- C)-(C -5-) bromo-(M-chlorobenzoic acid) (by machine translation)

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Paragraph 0012; 0017-0018, (2020/02/20)

The method sequentially comprises the following steps: a new, synthetic, route and a selective. reduction 2 - reaction are supplied to the preparation method of the anti.coccidiosis intermediate, and: the method sequentially comprises the following, steps

HORMONE RECEPTOR MODULATORS FOR TREATING METABOLIC CONDITIONS AND DISORDERS

-

Page/Page column 136; 137; 138, (2018/03/25)

The invention relates to activators of FXR useful in the treatment of autoimmune disorders, liver disease, intestinal disease, kidney disease, cancer, and other diseases in which FXR plays a role, having the Formula (I): (I), wherein L1, A, X1, X2, R1, R2, and R3 are described herein.

DMSO/I2 mediated C-C bond cleavage of α-ketoaldehydes followed by C-O bond formation: A metal-free approach for one-pot esterification

Venkateswarlu, Vunnam,Aravinda Kumar,Gupta, Sorav,Singh, Deepika,Vishwakarma, Ram A.,Sawant, Sanghapal D.

, p. 7973 - 7978 (2015/07/27)

A novel and efficient I2/DMSO mediated metal-free strategy is presented for the direct C-C bond cleavage of aryl-/heteroaryl- or aliphatic α-ketoaldehydes by C2-decarbonylation and C1-carbonyl oxidation to give the corresponding carboxylic acids followed by esterification in one pot, offering excellent yields in both the steps. Here, DMSO acts as the oxygen source/oxidant and this reaction works very well under both conventional heating and microwave irradiation. This is a very simple and convenient protocol.

AMIDE COMPOUNDS AS ION CHANNEL LIGANDS AND USES THEREOF

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Page/Page column 47-48, (2008/06/13)

Compounds are disclosed that have a formula represented by the following: The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, pain, inflammation, traumatic injury, and others.

Pesticidal compounds

-

, (2008/06/13)

Bicyclooctane pesticides of the formula are prepared by cyclisation of In these formulae R may be various organic groups and is preferably n-butyl or n-propyl while R2 is a polysubstituted phenyl group.

Use of Potassium Bromate: Bromination of Halobenzenes and Halobenzoic Acids

Banerjee, Amalendu,Banerjee, Gopal Chandra,Dutt, Sachchidananda,Banerjee, Santa (Mrs.),Samaddar, Haraprasad

, p. 640 - 642 (2007/10/02)

Syntheses of bromo compounds by the bromination of halobenzenes and halobenzoic acids using potassium bromate under acidic condition have been discussed.

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