ChemicalBook--->CAS DataBase List--->143269-74-3

143269-74-3

143269-74-3 Structure

143269-74-3 Structure
IdentificationMore
[Name]

3-Amino-4-chlorobenzoic acid hexadecyl ester
[CAS]

143269-74-3
[Synonyms]

3-AMINO-4-CHLORO BENZOIC ACID HEXADECYL ESTER
HEXADECYL 3-AMINO-4-CHLOROBENZOATE
3-Amino-4-chloro benzoic hexadecyl ester
3-AMINO-4-CHLOROBENZOICACIDHEXADECYLESTERAPPEARANCE
[EINECS(EC#)]

419-700-6
[Molecular Formula]

C23H38ClNO2
[MDL Number]

MFCD00186289
[Molecular Weight]

396.01
[MOL File]

143269-74-3.mol
Chemical PropertiesBack Directory
[Boiling point ]

495.5±25.0 °C(Predicted)
[density ]

1.017±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

1.48±0.10(Predicted)
[Appearance]

White to light yellow Solid
[CAS DataBase Reference]

143269-74-3(CAS DataBase Reference)
[EPA Substance Registry System]

Benzoic acid, 3-amino-4-chloro-, hexadecyl ester (143269-74-3)
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H312-H332
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501
[Hazard Codes ]

N
[Risk Statements ]

R51/53:Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment .
[Safety Statements ]

S61:Avoid release to the environment. Refer to special instructions safety data sheet .
[TSCA ]

TSCA listed
Raw materials And Preparation ProductsBack Directory
[Raw materials]

1-Bromohexadecane-->3-Amino-4-chlorobenzoic acid-->Water-->Potassium hydroxide-->Benzyltriethylammonium bromide-->Xylene
Hazard InformationBack Directory
[Chemical Properties]

White to light brown crystalline powder
[Synthesis]

A mixture of 16.3 g (0.132 moles) 45percent potassium hydroxide solution, 21.5 g (0.125 moles) of 3-amino-4-chlorobenzoic acid, 100 g of xylene, 40/3 g (0.132 moles) of 1-bromohexadecane and 4.5 g of benzyltriethylammonium bromide (10 mol percent) was heated to reflux. Water was removed using a Dean-Stark trap. After 3 hr at reflux (115-120° C.), the reaction was judged complete by tic. The reaction was cooled to 90° C. and washed with water to remove salts. The solvent was removed on a roto-vap, and the residue was crystallized from heptane to give 40.7 g (83 per cent yield) of a solid Hexadecyl 3-amino-4-chlorobenzoate.
[References]

[1] Patent: US2006/135807, 2006, A1. Location in patent: Page/Page column 3
[2] Patent: US2006/135807, 2006, A1. Location in patent: Page/Page column 2
Spectrum DetailBack Directory
[Spectrum Detail]

Hexadecyl 3-amino-4-chlorobenzoate(143269-74-3)1HNMR
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