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bis(3-allyl-4-oxo-3,4,5,6,7,8-hexahydrobenzothieno<2,3-d>pyrimidin-2-yl) disulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50629-10-2

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  • 50629-10-2 Structure
  • Basic information

    1. Product Name: bis(3-allyl-4-oxo-3,4,5,6,7,8-hexahydrobenzothieno<2,3-d>pyrimidin-2-yl) disulfide
    2. Synonyms: bis(3-allyl-4-oxo-3,4,5,6,7,8-hexahydrobenzothieno<2,3-d>pyrimidin-2-yl) disulfide
    3. CAS NO:50629-10-2
    4. Molecular Formula:
    5. Molecular Weight: 554.782
    6. EINECS: N/A
    7. Product Categories: N/A
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: bis(3-allyl-4-oxo-3,4,5,6,7,8-hexahydrobenzothieno<2,3-d>pyrimidin-2-yl) disulfide(CAS DataBase Reference)
    10. NIST Chemistry Reference: bis(3-allyl-4-oxo-3,4,5,6,7,8-hexahydrobenzothieno<2,3-d>pyrimidin-2-yl) disulfide(50629-10-2)
    11. EPA Substance Registry System: bis(3-allyl-4-oxo-3,4,5,6,7,8-hexahydrobenzothieno<2,3-d>pyrimidin-2-yl) disulfide(50629-10-2)
  • 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: 50629-10-2(Hazardous Substances Data)

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50629-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50629-10-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,2 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 50629-10:
(7*5)+(6*0)+(5*6)+(4*2)+(3*9)+(2*1)+(1*0)=102
102 % 10 = 2
So 50629-10-2 is a valid CAS Registry Number.

50629-10-2Downstream Products

50629-10-2Relevant academic research and scientific papers

ACYLATION AND BROMINATION OF SOME 2-MERCAPTOTHIENOPYRIMIDINONES AND SYNTHESIS OF THEIR 2-AMINO DERIVATIVES

Khripak, S. M.,Yakubets, V. I.,Dobosh, A. A.

, p. 1091 - 1094 (2007/10/02)

The acylation of 2-thio-3-R-4-oxo-3,4-dihydrothieno-pyrimidines by means of benzoyl chloride was studied.Depending on the reaction conditions, it may take place with formation of S-substituted and N-substituted derivatives.The bromination of the sodium salts of thienopyrimidines and their S- and N-substituted derivatives is accompanied by the formation of disulfides, which do not react with electrophilic reagents but react with amines to give 2-amino derivatives of thienopyrimidines.

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