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4265-49-0

Acetic acid, 2,2'-[(phenylmethylene)bis(thio)]bis- (9CI), also known as Thiodipropionic acid or 3,3'-Dithiodipropionic acid, is an organic compound with the chemical formula C10H12O4S2. It is a colorless crystalline solid that is soluble in water and ethanol. Acetic acid,2,2'-[(phenylmethylene)bis(thio)]bis- (9CI) is characterized by the presence of two acetic acid moieties connected through a phenylmethylene group, with each acetic acid unit having a sulfur atom attached to the alpha carbon. Thiodipropionic acid is used in various applications, including as a chelating agent, a stabilizer in rubber and plastics, and in the synthesis of other organic compounds. It is also known for its antioxidant properties and has been studied for potential use in the treatment of certain medical conditions.

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  • 4265-49-0 Structure

  • Basic information

    1. Product Name: Acetic acid,2,2'-[(phenylmethylene)bis(thio)]bis- (9CI)
    2. Synonyms: Aceticacid, (benzylidenedithio)di- (6CI,7CI,8CI); NSC 65451
    3. CAS NO:4265-49-0
    4. Molecular Formula: C11H12 O4 S2
    5. Molecular Weight: 272.346
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 4265-49-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 479.6°Cat760mmHg
    3. Flash Point: 243.9°C
    4. Appearance: N/A
    5. Density: 1.435g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Acetic acid,2,2'-[(phenylmethylene)bis(thio)]bis- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetic acid,2,2'-[(phenylmethylene)bis(thio)]bis- (9CI)(4265-49-0)
    11. EPA Substance Registry System: Acetic acid,2,2'-[(phenylmethylene)bis(thio)]bis- (9CI)(4265-49-0)

  • 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: 4265-49-0(Hazardous Substances Data)

4265-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4265-49-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,6 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4265-49:
(6*4)+(5*2)+(4*6)+(3*5)+(2*4)+(1*9)=90
90 % 10 = 0
So 4265-49-0 is a valid CAS Registry Number.

4265-49-0Relevant articles and documents

Solvent-free mechanochemical synthesis of bisthioglycolic acid derivatives: an efficient and versatile strategy for carbon–sulfur bond formation

Bhargava, Gaurav,Kumar, Rupesh,Naikoo, Rayees Ahmad,Singh, Parvesh

, (2021/10/07)

An eco-friendly, easily achievable and efficient strategy has been explored to synthesize functionalized bisthioglycolic acids using a variety of aldehydes and thioglycolic acid. The employed protocol is solvent free and provides the desirable products in

Syntheses of some novel and symmetrical bis(4-amino-4H-1,2,4-triazole-3- thiols)

Ebrahimi, Sattar,Sayadi, Masoomeh

, p. 647 - 652 (2013/02/22)

A series of bis(4-amino-4H-1,2,4-triazole-3-thiols) 3a-e were prepared by condensation reactions of 2,2-(phenylmethylene)bis(sulfanediyl)diacetic acids 2a-e with thiocarbohydrazide. The starting diacid 2a-e was prepared by reactions of aromatic aldehydes

SYNTHESIS, SPECTRAL STUDIES AND C-S BOND FISSION THROUGH PUMMERER REACTION OF SOME ALKYLDIACETATES

Gohar, Gamal A.

, p. 171 - 178 (2007/10/02)

A series of methyl and ethyldiacetates have been synthesized and their structures were identified.Correlation between δ-values of the benzylidene protons and ?-Hammett values has been found.The internal chemical shift Δν of the methylene protons was found to be correlated linearly with ?-Hammett constants indicating that the sulfur atom could transmit a polar effect to the substituent.Studies of H2O2 oxidation suggested that a competition between Pummerer and elimination reactions of the intermediate was involved. Key words: Benzylidene dithio diacetates; (1)HNMR spectra; Pummerer reaction

142. Praeparative chromatographische Enantiomerentrennung von synthetisch nuetzlichen cyclischen Acetalen

Seebach, Dieter,Mueller, Stefan G.,Gysel, Urs,Zimmermann, Juerg

, p. 1303 - 1318 (2007/10/02)

Preparative Chromatographic Resolution of Sunthetically Useful Cyclic Acetals Racemic cyclic acetals derived from aldehydes and glycine, glycolic acid, thioglycolic acid, formylacetic acid, and acetoacetic acid (oxazolidinones 4-13, dioxolanones 14,15, ox

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