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Cas Database

53673-16-8

53673-16-8

Identification

  • Product Name:N-(2-AMINOETHYL)-2-METHYLPROPANAMIDE

  • CAS Number: 53673-16-8

  • EINECS:

  • Molecular Weight:130.19

  • Molecular Formula: C6H14N2O

  • HS Code:2924199090

  • Mol File:53673-16-8.mol

Synonyms:N-(2-AMINOETHYL)-2-METHYLPROPANAMIDE

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Safety information and MSDS view more

  • Signal Word:no data available

  • Hazard Statement:no data available

  • First-aid measures: General adviceConsult a physician. Show this safety data sheet to the doctor in attendance.If inhaled If breathed in, move person into fresh air. If not breathing, give artificial respiration. Consult a physician. In case of skin contact Wash off with soap and plenty of water. Consult a physician. In case of eye contact Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician. If swallowed Never give anything by mouth to an unconscious person. Rinse mouth with water. Consult a physician.

  • Fire-fighting measures: Suitable extinguishing media Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide. Wear self-contained breathing apparatus for firefighting if necessary.

  • Accidental release measures: Use personal protective equipment. Avoid dust formation. Avoid breathing vapours, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust. For personal protection see section 8. Prevent further leakage or spillage if safe to do so. Do not let product enter drains. Discharge into the environment must be avoided. Pick up and arrange disposal. Sweep up and shovel. Keep in suitable, closed containers for disposal.

  • Handling and storage: Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Avoid exposure - obtain special instructions before use.Provide appropriate exhaust ventilation at places where dust is formed. For precautions see section 2.2. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.

  • Exposure controls/personal protection:Occupational Exposure limit valuesBiological limit values Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and at the end of workday. Eye/face protection Safety glasses with side-shields conforming to EN166. Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU). Skin protection Wear impervious clothing. The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace. Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique(without touching glove's outer surface) to avoid skin contact with this product. Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices. Wash and dry hands. The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and the standard EN 374 derived from it. Respiratory protection Wear dust mask when handling large quantities. Thermal hazards

Supplier and reference price

  • Manufacture/Brand
  • Product Description
  • Packaging
  • Price
  • Delivery
  • Purchase
  • Manufacture/Brand:American Custom Chemicals Corporation
  • Product Description:N-(2-AMINOETHYL)-2-METHYLPROPANAMIDE 95.00%
  • Packaging:1G
  • Price:$ 654.15
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Acrotein
  • Product Description:N-(2-Aminoethyl)-2-methylpropanamideHCl 97%
  • Packaging:0.5g
  • Price:$ 128.34
  • Delivery:In stock
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Relevant articles and documentsAll total 3 Articles be found

Colloid and nanosized catalysts in organic synthesis: XIII. Synthesis of 2-R-2-imidazolines catalyzed by copper and iron oxide nanoparticles

Popov,Mokhov,Kalitina

, p. 281 - 285 (2016/04/20)

The reaction of carboxylic acids with ethylenediamine catalyzed by copper or iron oxide nanoparticles proceeds at 80°C with azeotropic water distilling off during 2-8 h to form 2-R-2-imidazolines. Acyl and diacyl derivatives of ethylenediamine are formed in the reaction as side products.

Relationships between conformational behaviour and binding affinity towards β1 and β2 adrenoceptors of some chiral phenoxypropanolamines with bulky N-substituents

Villa,Villa,Pallavicini,Romeo,Valoti,Ferri,Iuliano,Brunello

, p. 643 - 658 (2007/10/03)

The optical isomers of a series of phenoxypropanolamine compounds with N-substituents bulkier than isopropyl have been synthesized, and their binding affinity towards β1 and β2-adrenoceptors has been determined. A computational study, including a Molecular Dynamics (MD) simulation and quenching in water and a GRID analysis provided some useful suggestions for possible interpretation patterns for the different affinity exhibited by the compounds studied.

New Histidyl amino acid derivatives, and pharmaceutical composition comprising the same

-

, (2008/06/13)

A compound of the formula: STR1 wherein R1 is lower alkyl optionally substituted with a substituent selected from the group consisting of acyl, hydroxy, lower alkoxy, aryl, lower alkylthio and a group of the formula: STR2 in which R5 is hydrogen or acyl and R6 is hydrogen or lower alkyl; aryl; or amino optionally substituted with substituent(s) selected from the group consisting of lower alkyl and acyl; and R2 is hydrogen or lower alkyl; or R1 and R2 are taken together with the attached nitrogen atom to form a heterocyclic group optionally substituted with substituent(s) selected from the group consisting of lower alkyl, hydroxy(lower )alkyl, lower alkoxy(lower)alkyl, acyl(lower)alkyl, oxo and acyl; R3 is hydrogen or lower alkyl; and R4 is lower alkyl; and its pharmaceutically acceptable salt, processes for the preparation thereof and pharmaceutical composition comprising the same.

Process route upstream and downstream products

Process route

ethylenediamine
107-15-3,85404-18-8

ethylenediamine

isobutyric Acid
79-31-2

isobutyric Acid

N-(2-aminoethyl)isobutyramide
53673-16-8

N-(2-aminoethyl)isobutyramide

C<sub>10</sub>H<sub>20</sub>N<sub>2</sub>O<sub>2</sub>

C10H20N2O2

2-(1-Methylethyl)-4,5-dihydro-1H-imidazol
40029-86-5

2-(1-Methylethyl)-4,5-dihydro-1H-imidazol

Conditions
Conditions Yield
With copper; In benzene; at 80 ℃; for 5h;
88%
N-(2-aminoethyl)isobutyramide
53673-16-8

N-(2-aminoethyl)isobutyramide

Conditions
Conditions Yield
With ethylenediamine; In ethyl acetate;
ethylenediamine
107-15-3,85404-18-8

ethylenediamine

Ethyl isobutyrate
97-62-1

Ethyl isobutyrate

N-(2-aminoethyl)isobutyramide
53673-16-8

N-(2-aminoethyl)isobutyramide

Conditions
Conditions Yield
unter Druck;
at 120 ℃; for 36h; Yield given;
ethylenediamine
107-15-3,85404-18-8

ethylenediamine

N-(2-aminoethyl)isobutyramide
53673-16-8

N-(2-aminoethyl)isobutyramide

Conditions
Conditions Yield
at 90 ℃;
ethylenediamine
107-15-3,85404-18-8

ethylenediamine

N-(2-aminoethyl)isobutyramide
53673-16-8

N-(2-aminoethyl)isobutyramide

Conditions
Conditions Yield
ethylenediamine
107-15-3,85404-18-8

ethylenediamine

isobutyric Acid
79-31-2

isobutyric Acid

N-(2-aminoethyl)isobutyramide
53673-16-8

N-(2-aminoethyl)isobutyramide

C<sub>10</sub>H<sub>20</sub>N<sub>2</sub>O<sub>2</sub>

C10H20N2O2

2-(1-Methylethyl)-4,5-dihydro-1H-imidazol
40029-86-5

2-(1-Methylethyl)-4,5-dihydro-1H-imidazol

Conditions
Conditions Yield
With copper; In benzene; at 80 ℃; for 5h;
88%
N-(2-aminoethyl)isobutyramide
53673-16-8

N-(2-aminoethyl)isobutyramide

Conditions
Conditions Yield
With ethylenediamine; In ethyl acetate;
ethylenediamine
107-15-3,85404-18-8

ethylenediamine

Ethyl isobutyrate
97-62-1

Ethyl isobutyrate

N-(2-aminoethyl)isobutyramide
53673-16-8

N-(2-aminoethyl)isobutyramide

Conditions
Conditions Yield
unter Druck;
at 120 ℃; for 36h; Yield given;
ethylenediamine
107-15-3,85404-18-8

ethylenediamine

N-(2-aminoethyl)isobutyramide
53673-16-8

N-(2-aminoethyl)isobutyramide

Conditions
Conditions Yield
at 90 ℃;
ethylenediamine
107-15-3,85404-18-8

ethylenediamine

N-(2-aminoethyl)isobutyramide
53673-16-8

N-(2-aminoethyl)isobutyramide

Conditions
Conditions Yield

Global suppliers and manufacturers

Global( 2) Suppliers
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  • Antimex Chemical Limied
  • Business Type:Lab/Research institutions
  • Contact Tel:0086-21-50563169
  • Emails:anthony@antimex.com
  • Main Products:163
  • Country:China (Mainland)
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