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Meso-2,3-Dibromosuccinic acid is a dibromoalkane carboxylic acid characterized by the presence of two bromine atoms attached to a succinic acid molecule. It is a chemical compound with unique properties due to the bromine atoms, making it useful in a range of chemical processes and applications.

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  • 608-35-5 Structure
  • Basic information

    1. Product Name: meso-2,3-Dibromosuccinic acid
    2. Synonyms: 2,3-Dibromo Dibutyric Acid;meso-2,3-Dibromosuccinic acid;Threo-2,3-Dibromo Dibutyric acid;Threo-2,3-Dibromobutanedioic acid
    3. CAS NO:608-35-5
    4. Molecular Formula: C4H4Br2O4
    5. Molecular Weight: 275.88
    6. EINECS: 208-396-9
    7. Product Categories: N/A
    8. Mol File: 608-35-5.mol
  • Chemical Properties

    1. Melting Point: 255-260℃
    2. Boiling Point: 262.4°C at 760 mmHg
    3. Flash Point: 112.5°C
    4. Appearance: /
    5. Density: N/A
    6. Vapor Pressure: 0.00323mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. Water Solubility: 20 g/L (17℃)
    11. CAS DataBase Reference: meso-2,3-Dibromosuccinic acid(CAS DataBase Reference)
    12. NIST Chemistry Reference: meso-2,3-Dibromosuccinic acid(608-35-5)
    13. EPA Substance Registry System: meso-2,3-Dibromosuccinic acid(608-35-5)
  • Safety Data

    1. Hazard Codes:  Xi:Irritant;
    2. Statements: R36/37/38:Irritating to eyes, respiratory system and skin.;
    3. Safety Statements: S24/25:Avoid contact with skin and eyes.;
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 608-35-5(Hazardous Substances Data)

608-35-5 Usage

Uses

Used in Organic Synthesis:
Meso-2,3-Dibromosuccinic acid is used as a reagent in organic synthesis for various reactions, including esterification and hydrolysis. Its unique properties contribute to the efficiency and selectivity of these reactions.
Used in Pharmaceutical Production:
Meso-2,3-Dibromosuccinic acid is utilized in the production of pharmaceuticals. Its presence in the synthesis process can enhance the properties of the final drug product, making it more effective or suitable for specific applications.
Used in Agrochemical Production:
Meso-2,3-Dibromosuccinic acid is also used in the production of agrochemicals. Its unique properties can contribute to the development of more effective and targeted agrochemicals for various agricultural applications.
Used in Fine Chemicals Production:
Meso-2,3-Dibromosuccinic acid is employed in the production of fine chemicals, where its unique properties can be leveraged to create high-quality specialty chemicals for various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 608-35-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 608-35:
(5*6)+(4*0)+(3*8)+(2*3)+(1*5)=65
65 % 10 = 5
So 608-35-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H4Br2O4/c5-1(3(7)8)2(6)4(9)10/h1-2H,(H,7,8)(H,9,10)/p-2/t1-,2+

608-35-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Meso-2,3-Dibromosuccinic Acid

1.2 Other means of identification

Product number -
Other names (2R,3S)-2,3-Dibromosuccinic 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:608-35-5 SDS

608-35-5Relevant articles and documents

Synthesis method of o-Dibromo compound

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Paragraph 0060-0067, (2022/01/04)

The present invention discloses a synthesis method of o-dibromo compounds, said synthesis method comprising the following steps: preparation of olefins, brominated salts and a mixed solution of bromate; to the mixed solution of dropwise addition of hydrochloric acid solution for reaction; to the end of the reaction, the extraction of o-dibromo compounds in the reaction product; the synthesis method to inexpensive brominated salts (industrial or recycled brominated salts) and bromate as a bromine source, enhance the full use of applicable resources; after the end of the reaction after a simple filtration treatment to obtain a sufficient purity of the product, It can reduce production costs; at the same time, facilitate the transportation and storage of raw materials, and improve the working environment. The synthesis method of the present invention is simple and easy to operate, high safety, small pollution, simple post-treatment, low production cost, product yield and purity can meet the production needs, is both cost advantages and safety and environmental advantages of the industrializable process.

Preparation method of butynedioic acid

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Paragraph 0050-0051, (2020/07/21)

The invention discloses a preparation method of butynedioic acid. The method comprises the following steps of: (1) firstly, carrying out water-free and oxygen-free treatment on a closed reaction kettle; (2) putting calcium carbide, a solvent, a catalyst and an auxiliary agent into the reaction kettle, introducing carbon dioxide into the reaction kettle, and heating and pressurizing for reaction; (3) separating the reacted mixture obtained in the step (2) to obtain a liquid mixture, and adding a KOH solution into the liquid mixture; stirring to separate out a white precipitate; and dissolving the white precipitate in hot water, acidifying with concentrated sulfuric acid, cooling, separating out the white precipitate, and filtering to obtain the product. The synthesis method disclosed by theinvention is relatively environment-friendly and low in production cost.

Preparation method of 1,3-dibenzyl-2-oxoimidazolidine-4,5-dicarboxylic acid

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Paragraph 0046; 0047; 0054; 0055; 0058-0063, (2017/08/30)

The invention relates to a preparation method of 1,3-dibenzyl-2-oxoimidazolidine-4,5-dicarboxylic acid, comprising the steps of subjecting fumaric acid, bromine and hydrobromic acid to additive reaction to generate meso-2,3-dDibromosuccinic acid, subjecting the meso-2,3-dDibromosuccinic acid, benzylamine and a strong base to aminating reaction to generate dibenzylamino salt, subjecting the dibenzylamino salt and triphosgene to cyclization to generate the 1,3-dibenzyl-2-oxoimidazolidine-4,5-dicarboxylic acid. The fumaric acid is subjected to addition, and then substitution and cyclization are performed to obtain the 1,3-dibenzyl-2-oxoimidazolidine-4,5-dicarboxylic acid, and detection shows that HPLC (high-performance liquid chromatography) content of the 1,3-dibenzyl-2-oxoimidazolidine-4,5-dicarboxylic acid may reach 98-99%. The preparation method has the advantages that hydrobromic acid is added for bromination additive reaction, the concentration and reaction temperature of the hydrobromic acid are optimized, and bromine loss is more reduced; amination mother liquid is used in amination, the cost is saved, and product yield is increased; in ring-closure reaction, pH and reaction product concentration are decreased, the yield of the 1,3-dibenzyl-2-oxoimidazolidine-4,5-dicarboxylic acid is increased greatly, and the quality of the 1,3-dibenzyl-2-oxoimidazolidine-4,5-dicarboxylic acid is improved; experiments verify that through process innovation, production cost is reduced greatly, production efficiency is improved, and the process is energy efficient and environmentally friendly.

Kinetic study of the Ce(III)-, Mn(II)-, or ferroin-catalyzed Belousov-Zhabotinsky reaction with pyruvic acid

Lin, Hsing-Lien,Yu, Yueh-O,Jwo, Jing-Jer

, p. 408 - 418 (2007/10/03)

Ce(III)-, Mn(II)-, or ferroin (Fe(phen)32+)-catalyzed reaction of bromate ion and pyruvic acid (PA) or its dimer exhibits oscillatory behavior. Both the open-chain dimer (parapyruvic acid, γ-methyl-γ-hydroxyl-α-keto-glutaric acid, DP

Synthesis of Pyrazinamide

Rao, A. V. Rama,Yadav, J. S.,Ravichandran, K.,Sahasrabudhe, A. B.,Chaurassia, S. S.

, p. 850 (2007/10/02)

The key intermediate, pyrazinoic acid (III) in the synthesis of pyrazinamide has been prepared starting from 2,3-dibromsuccinic acid.

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