77697-86-0 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
It is derived from propanediol, which is a three-carbon diol.
Explanation
The compound has a methylamino (-NHCH3) functional group attached to it.
Explanation
It is utilized in various industries due to its unique properties.
Explanation
It is used in research and development for the synthesis of other organic compounds.
Explanation
The compound is known for its wide range of applications across different industries.
Explanation
It serves as a building block or intermediate in the creation of other chemicals.
Explanation
Based on its molecular weight and structure, it is expected to be a liquid under normal conditions.
Explanation
Due to the presence of polar and nonpolar functional groups, it is likely to dissolve in both water and organic solvents.
Explanation
The presence of the amine and alcohol functional groups allows it to undergo various chemical reactions, such as substitution, addition, and condensation reactions.
Derivative of propanediol
Yes
Contains a methylamino group
Yes
Common uses
Pharmaceutical production, cosmetic products, industrial solvents
Research chemical
Yes
Versatility
High
Synthesis
Used in the synthesis of other organic compounds
Physical state
Likely a liquid at room temperature
Solubility
Soluble in water and organic solvents
Reactivity
Can react with various reagents
Check Digit Verification of cas no
The CAS Registry Mumber 77697-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,9 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 77697-86:
(7*7)+(6*7)+(5*6)+(4*9)+(3*7)+(2*8)+(1*6)=200
200 % 10 = 0
So 77697-86-0 is a valid CAS Registry Number.
77697-86-0Relevant academic research and scientific papers
Synthesis and Hydrolytic Lability of α-Phenoxyacetamides Containing Hydroxy Groups in the N-alkyl Residue
Anelli, Pier Lucio,Brocchetta, Marino,Canipari, Sonia,Losi, Pietro,Manfredi, Giuseppe,et al.
, p. 135 - 142 (2007/10/03)
Secondary and tertiary amides of 3,5-biscarbonyl>phenoxyacetic acid bearing hydroxy groups in positions β (β-OH) and γ (γ-OH) relative to the acetamide nitrogen atom have been synthesized.Such amides easily undergo cleavage of the acetamide bond in water at neutral pH.Hydrolysis rate constant for a series of such amides and protonation constants for the corresponding leaving amines were determined.No simple correlation between the two parameters could be found.A study of the dependence of these parameters on the structural features of the substrates, such as the presence of an N-methyl group and number of β-OH and γ-OH groups, was carried out.All these features lead to enhancement of the amide hydrolysis rate and a synergistic effect is operative when both N-methyl and β-OH groups are contained in the substrate.Presence of a methyl group increases the basicity of amines whereas β-OH and γ-OH groups have the opposite effect.Mechanistic speculations seem to indicate that the abnormal lability of the acetamide bond is due to protic-like catalysis by an intramolecular OH...N hydrogen bond.
