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CAS

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74321-69-0

S-Benzyl-N'-tert-butyl-N,N-dimethylisothioharnstoff is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74321-69-0 Structure

  • Basic information

    1. Product Name: S-Benzyl-N'-tert-butyl-N,N-dimethylisothioharnstoff
    2. Synonyms:
    3. CAS NO:74321-69-0
    4. Molecular Formula:
    5. Molecular Weight: 250.408
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74321-69-0.mol

  • 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: S-Benzyl-N'-tert-butyl-N,N-dimethylisothioharnstoff(CAS DataBase Reference)
    10. NIST Chemistry Reference: S-Benzyl-N'-tert-butyl-N,N-dimethylisothioharnstoff(74321-69-0)
    11. EPA Substance Registry System: S-Benzyl-N'-tert-butyl-N,N-dimethylisothioharnstoff(74321-69-0)

  • 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: 74321-69-0(Hazardous Substances Data)

74321-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74321-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,2 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74321-69:
(7*7)+(6*4)+(5*3)+(4*2)+(3*1)+(2*6)+(1*9)=120
120 % 10 = 0
So 74321-69-0 is a valid CAS Registry Number.

74321-69-0Downstream Products

74321-69-0Relevant articles and documents

Acylcarbodiimides, IV. Preparation and Some Reactions of Carbamoylcarbodiimides

Goerdeler, Joachim,Raddatz, Siegfried

, p. 1095 - 1105 (2007/10/02)

Starting from carbamoyl-thioureas (1) and with the aid of cyanuric trichloride/triethylamine several carbamoylcarbodiimides (2) were prepared.In the case of aryl-substituted 1, elimination of arylamine competed with that of hydrogen sulfide.Rearrangement of a guanyl isocyanate (6) formed in situ afforded 2a on another way.Many carbodiimides 2 add water and other protic nucleophiles very rapidly.The exact structure of the adducts 7 - 9 is discussed.

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