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2,3-diamino-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl naphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 81864-05-3 Structure
  • Basic information

    1. Product Name: 2,3-diamino-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl naphthalene
    2. Synonyms: 2,3-diamino-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl naphthalene
    3. CAS NO:81864-05-3
    4. Molecular Formula:
    5. Molecular Weight: 218.342
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 81864-05-3.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: 2,3-diamino-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl naphthalene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3-diamino-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl naphthalene(81864-05-3)
    11. EPA Substance Registry System: 2,3-diamino-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl naphthalene(81864-05-3)
  • 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: 81864-05-3(Hazardous Substances Data)

81864-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81864-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,8,6 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 81864-05:
(7*8)+(6*1)+(5*8)+(4*6)+(3*4)+(2*0)+(1*5)=143
143 % 10 = 3
So 81864-05-3 is a valid CAS Registry Number.

81864-05-3Relevant articles and documents

C-H Amination of Arenes with Hydroxylamine

See, Yi Yang,Sanford, Melanie S.

, p. 2931 - 2934 (2020)

This Letter describes the development of a TiIII-mediated reaction for the C-H amination of arenes with hydroxylamine. This reaction is applied to a variety of electron-rich (hetero)arene substrates, including a series of natural products and pharmaceuticals. It offers the advantages of mild conditions (room temperature), fast reaction rates (30 min), compatibility with ambient moisture and air, scalability, and the use of inexpensive commercial reagents.

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