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N-Acetyltyramine

N-Acetyltyramine structure

N-Acetyltyramine 

structure
  • CAS No:

    1202-66-0

  • Formula:

    C10H13NO2

  • Chemical Name:

    N-Acetyltyramine

  • Synonyms:

    Acetamide,N-[2-(4-hydroxyphenyl)ethyl]-;Acetamide,N-(p-hydroxyphenethyl)-;N-[2-(4-Hydroxyphenyl)ethyl]acetamide;N-Acetyltyramine;Tyramine,N-acetyl-;N-(4-Hydroxyphenethyl)acetamide

  • Categories:

    Organic Chemistry  >  Amides

Description

N-acetyltyramine is a member of the class of tyramines that is tyramine in which one of the hydrogens of the amino group is replaced by an acetyl group. It has a role as a marine metabolite, a bacterial metabolite, an Aspergillus metabolite, an animal metabolite and a quorum sensing inhibitor. It is a member of acetamides and a member of tyramines. It derives from a tyramine.

N-Acetyltyramine Basic Attributes

179.219

179.22

BZB50E9QVY

DTXSID60152731

2924299090

Characteristics

49.3

1.1

Off-White

1.122±0.06 g/cm3(Predicted)

169 °C

424.1±28.0 °C(Predicted)

210.3±24.0 °C

1.546

8.62E-08mmHg at 25°C

Safety Information

NONH for all modes of transport

3

26-39

Xi

P280-P305 + P351 + P338

H318

Drug Information

Acetamide, N-(p-hydroxyphenethyl)

N-Acetyltyramine Use and Manufacturing

Methods of Manufacturing

GK3-015 was prepared according to the following reaction scheme 12General procedure: To a solution of EXAMPLE 5 2-{4-[2-(4-Chlorobenzenesulphonylamino)-ethyl]-phenoxy}-2-methylpropionic acid A mixture of 44.8 g. (0.25 mol) GK3-015 was prepared according to the following reaction scheme 12GK3-015 was prepared according to the following reaction scheme 12The diacetyltyramine is now dissolved in 500 ml. methanol. 800 ml. (0.8 mol) 1 N aqueous potassium hydroxide solution are added dropwise thereto, the temperature thereby increasing to about 30 C., and then maintained for 2 hours at an internal temperature of 50 C. The reaction mixture is then cooled, rendered weakly acidic with concentrated hydrochloric acid and the methanol evaporated off in a vacuum. The product which crystallizes out is filtered off with suction, thoroughly washed with water and then dried. The yield of

Uses

N-[2-(4-Hydroxyphenyl)ethyl]acetamide maintains anti-tumor properties and is derived from a marine bacterium named Streptoverticillium. Cytotoxin.

Computed Properties

Molecular Weight:179.22
XLogP3:1.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:179.094628657
Monoisotopic Mass:179.094628657
Topological Polar Surface Area:49.3
Heavy Atom Count:13
Complexity:162
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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