2′-Aminoacetanilide

Modify Date: 2024-01-03 22:36:34

2′-Aminoacetanilide Structure
2′-Aminoacetanilide structure
Common Name 2′-Aminoacetanilide
CAS Number 34801-09-7 Molecular Weight 150.178
Density 1.2±0.1 g/cm3 Boiling Point 361.5±25.0 °C at 760 mmHg
Molecular Formula C8H10N2O Melting Point 133-137 °C(lit.)
MSDS Chinese USA Flash Point 172.4±23.2 °C
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name N-(2-aminophenyl)acetamide
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 361.5±25.0 °C at 760 mmHg
Melting Point 133-137 °C(lit.)
Molecular Formula C8H10N2O
Molecular Weight 150.178
Flash Point 172.4±23.2 °C
Exact Mass 150.079315
PSA 55.12000
LogP 0.13
Vapour Pressure 0.0±0.8 mmHg at 25°C
Index of Refraction 1.636
Storage condition 2-8°C

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi
Risk Phrases R36/37/38
Safety Phrases S26-S36
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924299090

 Synthetic Route

 Customs

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles2

More Articles
A short synthesis of phenanthro [2, 3-d] imidazoles from dehydroabietic acid. Application of the methodology as a convenient route to benzimidazoles. Fonseca T, et al.

Tetrahedron 57(9) , 1793-1799, (2001)

Cyclization of o-phenylenediamines by CO2 in the presence of H2 for the synthesis of benzimidazoles. Yu B, et al.

Green Chem. 15(1) , 95-99, (2013)

 Synonyms

MFCD00210388
o-acetylaminophenyl amine
N-acetyl-o-phenylenediamine
Acetanilide, 2-amino-
2'-Acetamidoaniline
Acetamide,N-(2-aminophenyl)
N-acetyl-1,2-phenylenediamine
N-(2-amino-phenyl)-acetamide
2′-Aminoacetanilide
Acetamide, N-(2-aminophenyl)-
2'-AMinoacetanilide
2-(Acetamido)aniline
[N-(2-aminophenyl)amino]acetamide
N-(2-Aminophenyl)acetamide
2-Aminoactanilide
2-Aminoacetanilide
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