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1569-96-6

Acetamide, N-(2-hydroxy-1,1-dimethylethyl)-, also known as tert-butyl acetoacetamide, is an organic compound with the chemical formula C7H13NO2. It is a colorless, crystalline solid that is soluble in water and various organic solvents. Acetamide, N-(2-hydroxy-1,1-dimethylethyl)- is primarily used as a chemical intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as a reagent in organic synthesis, particularly in the preparation of various esters and amides. Due to its versatile applications, tert-butyl acetoacetamide is an important compound in the field of organic chemistry.

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  • 1569-96-6 Structure

  • Basic information

    1. Product Name: Acetamide, N-(2-hydroxy-1,1-dimethylethyl)-
    2. Synonyms:
    3. CAS NO:1569-96-6
    4. Molecular Formula: C6H13NO2
    5. Molecular Weight: 131.175
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1569-96-6.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: Acetamide, N-(2-hydroxy-1,1-dimethylethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetamide, N-(2-hydroxy-1,1-dimethylethyl)-(1569-96-6)
    11. EPA Substance Registry System: Acetamide, N-(2-hydroxy-1,1-dimethylethyl)-(1569-96-6)

  • 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: 1569-96-6(Hazardous Substances Data)

1569-96-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1569-96-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1569-96:
(6*1)+(5*5)+(4*6)+(3*9)+(2*9)+(1*6)=106
106 % 10 = 6
So 1569-96-6 is a valid CAS Registry Number.

1569-96-6Relevant articles and documents

Decomposition of alkene adducts of thianthrene cation radical in nitrile solvents. Formation of alkyl-2-oxazolines and a new class of four-component products: 5-[(1-alkoxyalkylidene) ammonio]alkylthianthrenium diperchlorates

Shine, Henry J.,Zhao, Bing-Jun,Marx, John N.,Ould-Ely, Teyeb,Whitmire, Kenton H.

, p. 9255 - 9261 (2004)

The monoadducts (4a-d) of thianthrene cation radical perchlorate (1a) and isobutene, 2-methyl-butene, 2-methyl-2-butene, and 2-methylpentene decompose spontaneously in acetonitrile (MeCN) solution, with the formation of thianthrene (Th). Decomposition of 4a (1,2-(5,10-thianthreniumdiyl)-2-methylpropane diperchlorate) and 4a', the corresponding dihexafluorophosphate, was studied in depth and extensively with 1H and 13C NMR spectroscopy. Decomposition of 4a was found to involve the solvent itself as well as water in the solvent, remaining from incomplete drying, and gave, apart from Th, successively, the perchlorate salts of 2,4,4-trimethyl-2-oxazoline (6) and 2-amino-2-methylpropyl acetate (7). These salts, 6-HCIO4 and 7-HCIO4, respectively, were prepared and used in understanding the reactions of 4a as well as the relationships among 6, 7, and 2-(acetylamino)-2-methyl propanol (8) in acidified MeCN solution. Decompositions of 4a-d in MeCN and other nitriles (RCN) containing an added alcohol (ROH) led to new products, 5-[(1-alkoxyalkylidene)ammonio]alkylthianthrenium diperchlorates (5a-u). These compounds were identified with 1H and 13C NMR spectroscopy and, in part, with X-ray crystallography and elemental analysis. The mechanisms of formation of 5-7 are discussed.

METHOD OF MAKING A COMPOSITION OF AN ALKANOLAMINE ALKYLAMIDE AND A POLYOL

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Paragraph 0070, (2017/08/22)

The disclosure generally provides methods for preparing compositions comprising alkanolamine alkylamides and polyols. This disclosure further relates to methods for preparing compositions comprising alkanolamine alkylamides and polyols that can be used in formulations that provide moisturization.

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