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BENZOPHENONE-2,4,5-TRICARBOXYLIC ACID is a benzophenone derivative with the molecular formula C15H9O6, belonging to the class of aromatic carboxylic acids. It is known for its high thermal stability and is commonly used in the synthesis of polymers and as a building block for various organic compounds.

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  • 135989-69-4 Structure
  • Basic information

    1. Product Name: BENZOPHENONE-2,4,5-TRICARBOXYLIC ACID
    2. Synonyms: 2,4,5-Tricarboxybenzophenone;5-Benzoyl-1,2,4-benzenetricarboxylic acid;BENZOPHENONE-2,4,5-TRICARBOXYLIC ACID;5-BENZOYLBENZENE-1,2,4-TRICARBOXYLIC ACID
    3. CAS NO:135989-69-4
    4. Molecular Formula: C16H10O7
    5. Molecular Weight: 314.25
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135989-69-4.mol
  • Chemical Properties

    1. Melting Point: 224℃
    2. Boiling Point: 637℃
    3. Flash Point: 353℃
    4. Appearance: /
    5. Density: 1.531
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.672
    8. Storage Temp.: N/A
    9. Solubility: soluble in Methanol
    10. PKA: 2.47±0.10(Predicted)
    11. CAS DataBase Reference: BENZOPHENONE-2,4,5-TRICARBOXYLIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: BENZOPHENONE-2,4,5-TRICARBOXYLIC ACID(135989-69-4)
    13. EPA Substance Registry System: BENZOPHENONE-2,4,5-TRICARBOXYLIC ACID(135989-69-4)
  • 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: 135989-69-4(Hazardous Substances Data)

135989-69-4 Usage

Uses

Used in Polymer Synthesis:
BENZOPHENONE-2,4,5-TRICARBOXYLIC ACID is used as a monomer in the production of polymers, contributing to the development of materials with enhanced properties such as heat resistance and chemical stability.
Used in Organic Compounds Synthesis:
BENZOPHENONE-2,4,5-TRICARBOXYLIC ACID serves as a building block for the synthesis of various organic compounds, enabling the creation of new molecules with potential applications in different industries.
Used in Photopolymerization Reactions:
BENZOPHENONE-2,4,5-TRICARBOXYLIC ACID is used as a photoinitiator in photopolymerization reactions, where it absorbs light and initiates the curing process of light-sensitive materials, allowing for the rapid and efficient production of polymers under controlled conditions.
Used in Heat-Resistant Materials Production:
Due to its high thermal stability, BENZOPHENONE-2,4,5-TRICARBOXYLIC ACID is utilized in the production of heat-resistant materials, which can withstand high temperatures and are suitable for applications in harsh environments.

Check Digit Verification of cas no

The CAS Registry Mumber 135989-69-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,9,8 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135989-69:
(8*1)+(7*3)+(6*5)+(5*9)+(4*8)+(3*9)+(2*6)+(1*9)=184
184 % 10 = 4
So 135989-69-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H10O7/c17-13(8-4-2-1-3-5-8)9-6-11(15(20)21)12(16(22)23)7-10(9)14(18)19/h1-7H,(H,18,19)(H,20,21)(H,22,23)

135989-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzophenone-2,4,5-tricarboxylic Acid

1.2 Other means of identification

Product number -
Other names 5-Benzoylbenzene-1,2,4-tricarboxylic Acid

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:135989-69-4 SDS

135989-69-4Relevant articles and documents

Synthesis of protected derivatives and short peptides of antAib, a novel Cα-tetrasubstituted α-amino acid of the Ac5c type possessing a fused anthracene fluorophore

Lohier, Jean-Fran?ois,Wright, Karen,Peggion, Cristina,Formaggio, Fernando,Toniolo, Claudio,Wakselman, Michel,Mazaleyrat, Jean-Paul

, p. 6203 - 6213 (2007/10/03)

The Nα-Boc and Nα-Fmoc protected derivatives of 2-amino-2,3-dihydro-1H-cyclopenta[b]anthracene-2-carboxylic acid (antAib), a novel fluorescent, achiral, α-amino acid, rigid analogue of the known 9-antAla and 2-antAla residues, and be

Tetraanthraquinonoporphyrazines: I. Substituted 2,3-dicarboxyanthraquionones

Borisov,Maizlish,Shaposhnikov

, p. 1151 - 1156 (2007/10/03)

New procedures were developed for preparing substituted 2,3-dicarboxyanthraquinones by acylation of arenes with pyromellitic anhydride, followed by intramolecular cyclization of the products. The 2,3-dicarboxyanthraquinones prepared were further modified by oxidation, sulfonation, nitration, and reduction. 2005 Pleiades Publishing, Inc.

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