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2-acetamidoethyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 16180-96-4 Structure
  • Basic information

    1. Product Name: 2-acetamidoethyl acetate
    2. Synonyms: 2-acetamidoethyl acetate;N-[2-(Acetyloxy)ethyl]acetamide;Acetamide, N-(2-(acetyloxy)ethyl)-;Einecs 240-317-3;N-(2-ACETOXYETHYL)ACETAMIDE
    3. CAS NO:16180-96-4
    4. Molecular Formula: C6H11NO3
    5. Molecular Weight: 145.15644
    6. EINECS: 240-317-3
    7. Product Categories: N/A
    8. Mol File: 16180-96-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 301.1°Cat760mmHg
    3. Flash Point: 135.9°C
    4. Appearance: /
    5. Density: 1.059g/cm3
    6. Vapor Pressure: 0.00108mmHg at 25°C
    7. Refractive Index: 1.428
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-acetamidoethyl acetate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-acetamidoethyl acetate(16180-96-4)
    12. EPA Substance Registry System: 2-acetamidoethyl acetate(16180-96-4)
  • 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: 16180-96-4(Hazardous Substances Data)

16180-96-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16180-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,8 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16180-96:
(7*1)+(6*6)+(5*1)+(4*8)+(3*0)+(2*9)+(1*6)=104
104 % 10 = 4
So 16180-96-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO3/c1-5(8)7-3-4-10-6(2)9/h3-4H2,1-2H3,(H,7,8)

16180-96-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-acetamidoethyl acetate

1.2 Other means of identification

Product number -
Other names 1-Acetoxy-2-acetylamino-aethan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16180-96-4 SDS

16180-96-4Downstream Products

16180-96-4Relevant articles and documents

Method using amide ester to prepare diamine derivative

-

Paragraph 0064; 0065; 0066; 0067, (2018/10/19)

The invention provides a method using amide ester to prepare a diamine derivative. The method is characterized in that ester groups in amide esters containing both amide and ester functional groups are substituted to prepare the diamine derivative, and one of the diamine groups of the diamine derivative is carboxylic acid amide reserved from the amide ester raw materials. The method is cheap in raw material, easy in raw material obtaining, low in catalyst use amount, simple in reaction conditions and high in product stereoselectivity.

Silica-supported boric acid catalyzed synthesis of dihydropyrimidin-2-ones, bis(indolyl)methanes, esters and amides

Kumar, Vishal,Singh, Chitra,Sharma, Upendra,Verma, Praveen K.,Singh, Bikram,Kumar, Neeraj

, p. 83 - 89 (2014/02/14)

Silica-supported boric acid (H3BO3-SiO2) has been established as a green, efficient and recyclable catalyst for the synthesis of dihydropyrimidin-2-ones, bis(indolyl)methanes, and acetylation of alcohols, phenols, amines and thiols under solvent free conditions. The main features of the present method include clean reaction, mild conditions, low loading of environment friendly catalyst and easy workup procedure. The catalyst can be recycled at least five times without any significant loss in activity.

Sulfonylation-induced N-to O -Acetyl migration in 2-acetamidoethanol derivatives

Yamaguchi, Takao,Hesek, Dusan,Lee, Mijoon,Oliver, Allen G.,Mobashery, Shahriar

supporting information; experimental part, p. 3515 - 3517 (2010/08/03)

The first example of sulfonylation-induced N- to O-acetyl migration of 2-acetamidoethanol derivatives is described. This type of reaction could happen with any 2-acetamidoethanol derivatives under typical sulfonylation conditions (TsCl or MsCl, pyridine) and might be a common side reaction of significance. Furthermore, the results reveal that 2-acetamidoethanol derivatives with a sterically encumbered hydroxyl group result in the migration products in high yields. The mechanism of the migration reaction is discussed.

A Novel Series of N-(1-Aminoalkylidene)carboximidamides as Potential Hypoglycemic Agents

Breslin, Henry J.,Kukla, Michael J.,Tuman, Robert W.,Rebarchak, Mary C.,Bowden, Charles R.

, p. 1597 - 1603 (2007/10/02)

Nitrogen heterocyclic carboximidamides, such as linogliride, 1a, have been shown to possess significant hypoglycemic activity and have shown clinical efficacy as potential antidiabetic agents.We evaluated the biological significance of the heterocyclic ring A of general structure 1, which has always been maintained in this class of compounds, by preparing acyclic compounds of general structure 2.Preliminary in vivo biological testing, i.e., the glucose tolerance test in rats, indicates that a number of the specific acyclic carboximidamides prepared, 6a-6kk, possessed significant hypoglycemic activity often comparable to, and in some cases better than, the activity noted for our model compound, 1a.These results suggest that the heterocyclic ring A of 1 is not essential for hypoglycemic activity for this class of compounds.

Acetyl transfer reactions on AlPO4-Al2O3

Costa, Antonio,Riego, Juan Martin

, p. 2327 - 2328 (2007/10/02)

An efficient acetylation of alcohols and aliphatic amines promoted by the AlPO4-Al2O3/ethyl acetate system is described.The solid catalist acts, at least in part, as the acetyl carrier.

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