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CAS

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1337958-87-8

DiMethyl 2,5-dibromoIsophthalate, a chemical compound with the molecular formula C10H8Br2O4, is a white to off-white crystalline solid. It is a derivative of isophthalic acid, characterized by the presence of bromine substituents that make it a valuable building block for the synthesis of complex organic molecules. Due to its potential hazards, it requires careful handling and disposal to protect human health and the environment.

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  • 1337958-87-8 Structure

  • Basic information

    1. Product Name: DiMethyl 2,5-dibroMoisophthalate
    2. Synonyms: DiMethyl 2,5-dibroMoisophthalate
    3. CAS NO:1337958-87-8
    4. Molecular Formula: C10H8Br2O4
    5. Molecular Weight: 351.97612
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1337958-87-8.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.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: DiMethyl 2,5-dibroMoisophthalate(CAS DataBase Reference)
    10. NIST Chemistry Reference: DiMethyl 2,5-dibroMoisophthalate(1337958-87-8)
    11. EPA Substance Registry System: DiMethyl 2,5-dibroMoisophthalate(1337958-87-8)

  • 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: 1337958-87-8(Hazardous Substances Data)

1337958-87-8 Usage

Uses

Used in Pharmaceutical Industry:
DiMethyl 2,5-dibromoIsophthalate is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure and bromine substituents contribute to the development of new drugs with specific therapeutic properties.
Used in Dye Industry:
In the dye industry, DiMethyl 2,5-dibromoIsophthalate serves as a key intermediate for the production of dyes with specific color characteristics and properties. Its chemical structure allows for the creation of dyes with improved stability and performance.
Used in Organic Compounds Synthesis:
DiMethyl 2,5-dibromoIsophthalate is used as a building block in the synthesis of other organic compounds. Its versatility and reactivity make it a valuable component in the creation of a wide range of organic molecules for various applications, including chemical research and industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1337958-87-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,7,9,5 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1337958-87:
(9*1)+(8*3)+(7*3)+(6*7)+(5*9)+(4*5)+(3*8)+(2*8)+(1*7)=208
208 % 10 = 8
So 1337958-87-8 is a valid CAS Registry Number.

1337958-87-8SDS

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 dimethyl 2,5-dibromobenzene-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names Dimethyl 2,5-dibromoisophthalate

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:1337958-87-8 SDS

1337958-87-8Relevant articles and documents

Apical functionalization of chiral heterohelicenes

Surampudi, Sravan K.,Nagarjuna,Okamoto, Daiki,Chaudhuri, Piyali D.,Venkataraman

, p. 2074 - 2079 (2012/03/27)

We describe a synthetic protocol to selectively functionalize chiral bridged triarylamines at the apical position using regioselective copper-catalyzed amination reaction. This protocol allows the coupling of diphenylamines with a sterically hindered but

Process for the preparation of bromoisophthalic acid compounds

-

Page 4, (2010/02/05)

The present invention relates to a process for preparing bromoisophthalic acid compounds, particularly 5-bromoisophthalic acid compounds and 4,5-dibromoisophthalic acid compounds comprising brominating an isophthalic acid compound of the general formula (1) wherein R1 and R2 independently of one another are hydrogen atom or C1-6 alkyl, with bromine in a solvent containing sulfur trioxide. The object of the invention is to provide a process for preparing bromoisophthalic acid compounds, particularly 5-bromoisophthalic acid compounds and 4,5-dibromoisophthalic acid compounds in a highly selective manner by using bromine that is industrially inexpensive.

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