ChemicalBook--->CAS DataBase List--->1885-29-6

1885-29-6

1885-29-6 Structure

1885-29-6 Structure
IdentificationMore
[Name]

Anthranilonitrile
[CAS]

1885-29-6
[Synonyms]

2-AMINOBENZONITRILE
2-CYANANILINE
2-CYANOANILINE
AKOS 91125
AMINOBENZONITRILE(2-)
ANTHRANILIC ACID NITRILE
ANTHRANILONITRILE
LABOTEST-BB LTBB000570
O-AMINOBENZONITRILE
O-CYANOANILINE
2-amino-benzonitril
2-Cyano-1-aminobenzene
Benzonitrile, o-amino-
2-Aminobenzonitrile, (Anthranilonitrile
Aminobenzonitrile
Anthranilonitrile~2-Cyanoaniline
2-AMINO BENZONITRILE (2-CYANO ANILINE)
2-Aminobenzontrile
2-Aminoobenzonitrile
Benzonitrile, 2-amino-
[EINECS(EC#)]

217-549-9
[Molecular Formula]

C7H6N2
[MDL Number]

MFCD00007631
[Molecular Weight]

118.14
[MOL File]

1885-29-6.mol
Chemical PropertiesBack Directory
[Appearance]

Yellow Solid
[Melting point ]

45-48 °C (lit.)
[Boiling point ]

267-268 °C (lit.)
[density ]

1.11 g/cm3 (50℃)
[refractive index ]

1.5500 (estimate)
[Fp ]

>230 °F
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
[form ]

Crystalline Flakes
[pka]

0.77(at 25℃)
[color ]

Yellow to beige-brown
[Water Solubility ]

INSOLUBLE
[Usage]

Used for induction of nitrilase activity in Arthrobacter. Used as radioprotective agent
[BRN ]

907187
[InChI]

1S/C7H6N2/c8-5-6-3-1-2-4-7(6)9/h1-4H,9H2
[InChIKey]

HLCPWBZNUKCSBN-UHFFFAOYSA-N
[SMILES]

Nc1ccccc1C#N
[LogP]

0.901
[CAS DataBase Reference]

1885-29-6(CAS DataBase Reference)
[NIST Chemistry Reference]

Benzonitrile, 2-amino-(1885-29-6)
[EPA Substance Registry System]

1885-29-6(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H317-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352+P312-P304+P340+P312-P305+P351+P338
[Hazard Codes ]

Xn,T,Xi
[Risk Statements ]

R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
R43:May cause sensitization by skin contact.
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37:Wear suitable protective clothing and gloves .
S36:Wear suitable protective clothing .
[RIDADR ]

3276
[WGK Germany ]

2
[RTECS ]

CB4575000
[TSCA ]

T
[REACH Registrations]

Active
[HazardClass ]

6.1
[PackingGroup ]

III
[HS Code ]

29269095
[Storage Class]

13 - Non Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
Skin Sens. 1
STOT SE 3
[Toxicity]

LD50 ivn-mus: 180 mg/kg CSLNX* NX#00381
Raw materials And Preparation ProductsBack Directory
[Raw materials]

2-Nitrobenzonitrile-->Anthranilamide-->Phenylphosphonic dichloride
[Preparation Products]

1,2,3,4-Tetrahydro-9-acridinamine-->6-Chloroquinazolin-4-amine-->4-Chloro-2-chloromethylquinazoline-->2-Amino-5-chlorobenzonitrile-->2-Amino-thiobenzamide-->Ethyl 2-(2-cyanoanilino)acetate-->Pitavastatin Methyl Ester-->Quinazolin-4-ylamine-->2-Iodobenzamide-->ME0328-->3,5-Dibromobenzonitrile
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

2-Aminobenzonitrile(1885-29-6).msds
Hazard InformationBack Directory
[Chemical Properties]

2-Aminobenzonitrile(1885-29-6) is a chemically stable yellow solid that readily forms salts when it encounters acid. It can be oxidized to nitrogen oxide by oxidants but has certain toxicity. The substance is easily soluble in common organic solvents but hardly soluble in low-polarity solvents, and it is insoluble in water.
[Uses]

2-Aminobenzonitrile is used for induction of nitrilase activity in Arthrobacter and for radioprotective agent.
[Preparation]

Synthesis of 2-Aminobenzonitrile: 2-Aminobenzamide was dehydrated to 2-aminobenzonitrile without protection of the amino group in the presence of phenylphosphonyl dichloride and pyridine. The highest yield of 96% was obtained using reagent 2d, while reagents 2a-c yielded less than 60%.
Synthesis of 2-Aminobenzonitrile
The reagents used for the reaction included phosphoryl chloride (2a), phenyl phosphoryl dichloride (2b), 4-chlorophenyl phosphoryl dichloride (2c), and phenylphosphonic dichloride (2d) in pyridine.
synthesis of aminobenzonitrile by dehydration of aminobenzamide using phenylphosphonic dichloride in pyridine
[Synthesis Reference(s)]

Journal of the American Chemical Society, 96, p. 5933, 1974 DOI: 10.1021/ja00825a039
The Journal of Organic Chemistry, 43, p. 944, 1978 DOI: 10.1021/jo00399a030
Tetrahedron Letters, 32, p. 1007, 1991 DOI: 10.1016/S0040-4039(00)74473-X
Improving a process for the preparation of 2-aminobenzonitrile by reduction of 2-nitrobenzonitrile.
[Safety Profile]

Poison by intravenous route. Seealso NITRILES. When heated to decomposition it emitstoxic fumes of NOx and CN- .
Spectrum DetailBack Directory
[Spectrum Detail]

2-Aminobenzonitrile(1885-29-6)MS
2-Aminobenzonitrile(1885-29-6)1HNMR
2-Aminobenzonitrile(1885-29-6)13CNMR
2-Aminobenzonitrile(1885-29-6)IR1
2-Aminobenzonitrile(1885-29-6)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Anthranilonitrile, 98%(1885-29-6)
[Alfa Aesar]

2-Aminobenzonitrile, 98%(1885-29-6)
[Sigma Aldrich]

1885-29-6(sigmaaldrich)
[TCI AMERICA]

2-Aminobenzonitrile,>98.0%(GC)(1885-29-6)
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