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104733-02-0

2-benzyloxycarbonylphenyl 4-nitrophenyl sulphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104733-02-0 Structure

  • Basic information

    1. Product Name: 2-benzyloxycarbonylphenyl 4-nitrophenyl sulphate
    2. Synonyms:
    3. CAS NO:104733-02-0
    4. Molecular Formula:
    5. Molecular Weight: 429.407
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104733-02-0.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: 2-benzyloxycarbonylphenyl 4-nitrophenyl sulphate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-benzyloxycarbonylphenyl 4-nitrophenyl sulphate(104733-02-0)
    11. EPA Substance Registry System: 2-benzyloxycarbonylphenyl 4-nitrophenyl sulphate(104733-02-0)

  • 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: 104733-02-0(Hazardous Substances Data)

104733-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104733-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,3 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104733-02:
(8*1)+(7*0)+(6*4)+(5*7)+(4*3)+(3*3)+(2*0)+(1*2)=90
90 % 10 = 0
So 104733-02-0 is a valid CAS Registry Number.

104733-02-0Downstream Products

104733-02-0Relevant articles and documents

Intramolecular Catalysis of Sulphate Diester Hydrolysis by One and Two Carboxy Groups. The Hydrolysis of Aryl 2-Carboxyphenyl Sulphates

Drummond, Jeremy N.,Kirby, Anthony J.

, p. 579 - 584 (2007/10/02)

The hydrolysis of aryl 2-carboxyphenyl (salicyl) sulphates is subject to efficient nucleophilic catalysis by the neighbouring carboxylate group.The intermediate cyclic acyl sulphate can be trapped with hydroxylamine.The reaction of disalicyl sulphate is further catalysed by the second carboxy group, acting, rather inefficiently, as a general acid.

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