![]() 3-Aminobenzonitrile structure
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Common Name | 3-Aminobenzonitrile | ||
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CAS Number | 2237-30-1 | Molecular Weight | 118.136 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 290.0±13.0 °C at 760 mmHg | |
Molecular Formula | C7H6N2 | Melting Point | 48-53 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 129.2±19.8 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Name | 3-Aminobenzonitrile |
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Synonym | More Synonyms |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 290.0±13.0 °C at 760 mmHg |
Melting Point | 48-53 °C(lit.) |
Molecular Formula | C7H6N2 |
Molecular Weight | 118.136 |
Flash Point | 129.2±19.8 °C |
Exact Mass | 118.053101 |
PSA | 49.81000 |
LogP | 1.07 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.590 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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Symbol |
![]() GHS07 |
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Signal Word | Warning |
Hazard Statements | H302 + H312 + H332-H317 |
Precautionary Statements | P280 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Faceshields;Gloves |
Hazard Codes | Xn:Harmful; |
Risk Phrases | R22 |
Safety Phrases | S36/37 |
RIDADR | 3276 |
WGK Germany | 3 |
RTECS | DI2454000 |
Packaging Group | III |
Hazard Class | 6.1 |
HS Code | 2926909090 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2926909090 |
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Summary | HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0% |
Synthesis, anti-inflammatory and analgesic activities evaluation of some mono, bi and tricyclic pyrimidine derivatives.
Bioorg. Med. Chem. 13(22) , 6158-66, (2005) 3-Aminobenzonitrile and 2-amino-4-phenyl thiazole on condensation with 4-isothiocyanato-4-methyl pentane-2-one gave condensed monocyclic pyrimidine derivatives 1 and 2, 3, respectively. Condensation o... |
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Synthesis and biological evaluation of 1-substituted-3(5)-(6-methylpyridin-2-yl)-4-(quinoxalin-6-yl)pyrazoles as transforming growth factor-β type 1 receptor kinase inhibitors.
Eur. J. Med. Chem. 46(9) , 3917-25, (2011) A series of 1-substituted-3(5)-(6-methylpyridin-2-yl)-4-(quinoxalin-6-yl)pyrazoles 14a-d, 15a-d, 17a, 17b, 18a-d, 19a, and 19b has been synthesized and evaluated for their ALK5 inhibitory activity in ... |
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Preparation of highly substituted gamma-lactam follicle stimulating hormone receptor agonists.
Bioorg. Med. Chem. 13(21) , 5986-95, (2005) An unusual combination of Weinreb amidation and Mitsunobu lactam formation was used to prepare highly substituted gamma-lactam analogues of a thiazolidinone follicle stimulating hormone receptor agoni... |
3-Aminobenzonitrile |
1-amino-3-cyanobenzene |
3-Cyanoaniline |
3-Amino-benzonitrile |
Benzonitrile, 3-amino- |
M-AMINOBENZONITRILE |
m-Cyanoaniline |
MFCD00007756 |
3-aminobenzonitril |
EINECS 218-800-5 |
3-Aminobenzolcarbonitril |
3-cyanophenylamine |
Benzonitrile,3-amino |
m-cyanophenyl amine |
Benzonitrile,m-amino |
m-Anthranilonitrile |
meta-cyanoaniline |