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78053-04-0

1-Adamantan-1-yl-butan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 78053-04-0 Structure

  • Basic information

    1. Product Name: 1-Adamantan-1-yl-butan-1-ol
    2. Synonyms: 1-Adamantan-1-yl-butan-1-ol
    3. CAS NO:78053-04-0
    4. Molecular Formula:
    5. Molecular Weight: 208.344
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78053-04-0.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: 1-Adamantan-1-yl-butan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Adamantan-1-yl-butan-1-ol(78053-04-0)
    11. EPA Substance Registry System: 1-Adamantan-1-yl-butan-1-ol(78053-04-0)

  • 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: 78053-04-0(Hazardous Substances Data)

78053-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78053-04-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,5 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78053-04:
(7*7)+(6*8)+(5*0)+(4*5)+(3*3)+(2*0)+(1*4)=130
130 % 10 = 0
So 78053-04-0 is a valid CAS Registry Number.

78053-04-0Downstream Products

78053-04-0Relevant articles and documents

Preparation of 1-adamantyl ketones: Structure, mechanism of formation and biological activity of potential by-products

Vicha, Robert,Necas, Marek,Potacek, Milan

, p. 709 - 722 (2008/02/01)

Reactions between adamantane-1-carbonyl chloride and several Grignard reagents as well as interactions with solvents have been examined. Some new and unexpected adamantane derivatives were isolated, fully characterized and their biological activity determined. In particular, an unexpected isochromanone 16 was formed in an SEAr process, in which a stable hydrocarbon was the leaving group.

TRIFLUOROACETIC ANHYDRIDE AS A MEDIUM FOR ORGANIC REACTIONS. FUNCTIONAL SUBSTITUTION OF ADAMANTANE AND ITS DERIVATIVES

Kovalev, V. V.,Fedorova, O. A.,Shokova, E. A.

, p. 1672 - 1675 (2007/10/02)

The role of trifluoroacetic anhydride during the oxidation of adamantane and its derivatives with sulfuric acid was studied. 1-Adamantanol, 1-(4-methyl-3-nitrophenyl)-3-adamantanol.The latter was used without isolation from the reaction mixture for the production of 1-adamantanecarboxylic acid, N-(1-adamantyl)acetamide, 1-(1-adamantyl)butan-1-ol, 1-(4-methylphenyl)adamantane, 4-(1-adamantyl)phenoxyacetic acid, 4-(1-adamantyl)acetanilide, and 4-(1-adamantyl)bromobenzene.

Synthesis of 1-adamantyl and 1-adamantylmethyl alkyl ketones

Grava, I. Ya.,Polis, Ya. Yu.,Lidak, M. Yu.,Liepin'sh, E. E.,Shatts, V. D.,et al.

, p. 679 - 686 (2007/10/02)

The reaction of 1-adamantanecarboxylic and 1-adamantylacetic acids with Grignard reagents in the presence of cuprous chloride or iodide gave the corresponding ketones.

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